Medical Forum / Diseases and Disorders / AIDS / October 2005
Syphilis in the UK
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GMCarter - 14 Oct 2005 18:45 GMT http://sti.bmjjournals.com/cgi/content/full/80/3/159 Sex Transm Infect 2004;80:159-166 © 2004 BMJ Publishing Group Ltd EPIDEMIOLOGICAL REVIEW Recent trends in HIV and other STIs in the United Kingdom: data to the end of 2002 A E Brown1, K E Sadler1, S E Tomkins1, C A McGarrigle1, D S LaMontagne1, D Goldberg2, P A Tookey3, B Smyth4, D Thomas5, G Murphy6, J V Parry6, B G Evans1, O N Gill1, F Ncube1 and K A Fenton1,7
1 HIV and STI Department, Health Protection Agency, Communicable Disease Surveillance Centre, UK 2 The Scottish Centre for Infection and Environmental Health, UK 3 Institute of Child Health (ICH), University College London, UK 4 Health Protection Agency, Communicable Disease Surveillance Centre (Northern Ireland), UK 5 National Public Health Service for Wales, Communicable Disease Surveillance Centre, UK 6 The Sexually Transmitted and Blood Borne Viruses Laboratory, Specialist and Reference Microbiology Division, Health Protection Agency, UK 7 The Centre for Sexual Health and HIV Research, Department of Primary Care and Population Sciences, Royal Free and University College Medical School, London, UK
Correspondence to: Alison Brown HIV and STI Department, Communicable Disease Surveillance Centre, 61 Colindale Avenue, London NW9 5EQ, UK; alison.brown@hpa.org.uk
Accepted for publication 2 April 2004
ABSTRACT Sexual health in the United Kingdom has deteriorated in recent years with further increases in HIV and other sexually transmitted infections (STIs) reported in 2002. This paper describes results from the available surveillance data in the United Kingdom from the Health Protection Agency and its national collaborators. The data sources range from voluntary reports of HIV/AIDS from clinicians, CD4 cell count monitoring, a national census of individuals living with HIV, and the Unlinked Anonymous Programme, to statutory reports of STIs from genitourinary medicine (GUM) clinics and enhanced STI surveillance systems. In 2002, an estimated 49 500 adults aged over 15 years were living with HIV in the United Kingdom, of whom 31% were unaware of their infection. Diagnoses of new HIV infections have doubled from 1997 to 2002, mainly driven by heterosexuals who acquired their infection abroad. HIV transmission also continues within the United Kingdom, particularly among homo/bisexual men who, in 2002, accounted for 80% of all newly diagnosed HIV infections acquired in the United Kingdom. New diagnoses of syphilis have increased eightfold, and diagnoses of chlamydia and gonorrhoea have doubled from 1997 to 2002 overall; STI rates disproportionately affect homo/bisexual men and young people. Effective surveillance is essential in the provision of timely information on the changing epidemiology of HIV and other STIs; this information is necessary for the targeting of prevention efforts and through providing baseline information against which progress towards targets can be monitored.
Keywords: HIV; sexually transmitted infections; United Kingdom
Sexual health in the United Kingdom has deteriorated in recent years.1,2 Increases in HIV and other sexually transmitted infections (STIs) have placed enormous pressure on existing sexual health services.3 Consequent delays in accessing diagnosis and care may in turn be facilitating infection transmission. Since 2001, a range of new initiatives aimed at improving sexual health have been established in the United Kingdom. In England, the implementation of the 10 year National Strategy for Sexual Health and HIV 4 has seen the appointment of local sexual health leads in primary care trusts (PCTs) and the Independent Advisory Group on Sexual Health5; greater investment in genitourinary medicine (GUM) clinics, and phased implementation of prevention interventions, such as the National Chlamydia Screening Programme, aimed at specific population risk groups. There have been similar strategies in other UK countries (Wales,6 Scotland,7 and Northern Ireland).8 The Health Select Committee report on Sexual Health,9 the All Party Parliamentary Group on AIDS report on Migration and HIV,10 and most recently the governments response to the Health Select Committees report on sexual health11 have all drawn attention to the need for greater political will and investment in tackling HIV and STIs in the United Kingdom and globally.
Surveillance data have a key role in such strategies. The collection and analysis of data, in conjunction with the monitoring of trends with timely feedback provides information for the implementation and evaluation of these initiatives. Specifically, by highlighting where prevention efforts should be targeted and through providing baseline information against which progress towards targets can be monitored.
The immediate public health challenges facing sexual health in the United Kingdom include increasing incidence and prevalence of HIV and STIs; rising costs of HIV related care; variation in disease determinants and distribution; and the associated long term morbidity and mortality of these conditions. This paper summarises recent trends in the UK surveillance data for HIV and other STIs up until the end of 2002.12
DATA SOURCES In the United Kingdom, the majority of STIs, including HIV, are diagnosed and treated in GUM clinics which form part of the National Health Service. Although diagnoses of many STIs (particularly chlamydia) occur in primary care and other community settings,13 only GUM clinics have statutory reporting of STIs to the Health Protection Agency and its collaborators by clinicians. The detailed methods of the HIV and STI surveillance systems in the United Kingdom have been described elsewhere12 and are briefly summarised here.
HIV/AIDS reporting New diagnoses of HIV infections, AIDS cases, and deaths14 (HIV/AIDS reporting) are reported by laboratories and clinicians through voluntary reporting systems. The annual Survey of Prevalent HIV Infections Diagnosed (SOPHID)15 provides a census of the number of individuals living with diagnosed HIV infection and receiving care in England, Wales, and Northern Ireland. Longitudinal data on CD4 T lymphocytes16 (CD4 surveillance) are reported from laboratories in England, Wales and Scotland and are used to monitor trends in immunosuppression associated with HIV infection. In Scotland, these data are used to gauge the number of people in specialist HIV care.
Unlinked anonymous HIV surveys The unlinked anonymous (UA) HIV surveys17 measure the prevalence of HIV, including undiagnosed HIV infections, in selected subgroups of the population. The unlinked anonymous survey of GUM clinic attendees (UA GUM survey) measures HIV prevalence in a high risk population (attendees of sentinel GUM clinics in the United Kingdom).18 In England, Wales, and Northern Ireland the incidence of HIV infection in homo/bisexual men included in the UA GUM survey has been determined by application of the Serological Testing Algorithm for Recent HIV Seroconversion (STARHS).19
Prevalence in the general population is measured by surveys of pregnant women (UA pregnant women surveyspregnant women attending antenatal care and women giving birth in England and Scotland). Live births to diagnosed HIV infected women in the United Kingdom are reported to the National Study of HIV in Pregnancy and Childhood.20 These reports are aligned with the overall prevalence estimates for HIV in pregnant women by geographical area, to produce estimates of the proportion of women giving birth who were diagnosed before antenatal attendances, diagnosed through antenatal testing, and who remained undiagnosed at delivery.21
STI surveillance Statutory KC60 returns from all GUM clinics12 in England, Wales, and Northern Ireland provide aggregate data on the total episodes of diagnosed STIs by sex and age group (and sexual orientation for selected conditions). The ISD(D)5 returns system provides disaggregate data on all STI diagnoses in GUM clinics in Scotland.12 NHS laboratories throughout the United Kingdom provide voluntary electronic disaggregate reporting on laboratory diagnoses of selected STIs with age and sex information. Enhanced Syphilis Surveillance (ESS) collects further demographic and risk factor data in the United Kingdom, and is designed to improve interpretation of the incidence and distribution of infectious syphilis.22 The Gonococcal Resistance to Antimicrobials Surveillance Programme (GRASP) is a sentinel surveillance system for monitoring gonococcal antimicrobial resistance and collects detailed behavioural information on diagnoses of gonorrhoea in England.23
Related surveillance techniques Estimates of the total number of HIV infected people in the United Kingdom24 were calculated by combining data from SOPHID (for diagnosed HIV infections) and the unlinked anonymous surveys (for undiagnosed HIV infections), with estimates of the size of the population in various exposure categories derived from the National Survey of Sexual Attitudes and Lifestyles (Natsal 2000),25 and census 2001 population estimates (Office for National Statistics).
Annual rates (cases/population) of diagnoses of STIs were calculated per 100 000 people. The 2002 rates for all regions and countries in the United Kingdom were calculated by dividing the number of cases reported from GUM clinics in each area in 2002 by the mid-2002 population estimates from the Office for National Statistics (for homo/bisexual men population estimates were derived from Natsal 200025). Descriptive epidemiology is the focus of the paper, but hypothesis tests have been used to supplement the data where appropriate using Stata 7 (StataCorp, 2001).
Previously undiagnosed HIV infection
This includes both HIV infected individuals who were diagnosed with HIV at the episode of clinical care, and individuals who left clinical care remaining unaware of their infection, but excludes individuals whose HIV infection was diagnosed before the episode of clinical care
OVERALL HIV/STI SURVEILLANCE TRENDS Estimates of the total prevalent infections indicate that at the end of 2002, 49 500 adults aged over 15 were living with HIV in the United Kingdom, of whom 15 200 (31%) were unaware of their infection. There were 5542 new HIV diagnoses reported for 2002: double the 2735 diagnoses in 1997.
At the end of 2002, overall HIV prevalence among homo/bisexual men in the United Kingdom was estimated at 7%, with estimates of total prevalent infections indicating that 22 600 homo/bisexual men were infected with HIV, of whom 5500 (24%) were unaware of their infection. Of the newly diagnosed HIV infections that were acquired in the United Kingdom, 80% (1500/1850) were among homo/bisexual men. The UA GUM survey found 4% (27/672) of homo/bisexual men aged under 25 in London had a previously undiagnosed HIV infection in 2002, indicating continuing transmission in this population (fig 1A). Annual incidence in GUM attendees, measured using STARHS, rose to approximately 3.5% in 2002.26
View larger version (22K): [in this window] [in a new window] Figure 1 Prevalence of previously undiagnosed HIV infection in England, Wales, and Northern Ireland, 19932002. (A) Previously undiagnosed* HIV infection in homo/bisexual men{dagger} by clinical presentation and age group. (B) Previously undiagnosed* HIV infection in heterosexuals{dagger} and overall HIV prevalence in women giving birth. (*Excludes HIV infected attendees who were previously diagnosed.{dagger}Attendees at 15 GUM clinics in England, Wales, and Northern Ireland (seven in London, eight elsewhere). {ddagger}Acute STI is defined as presenting with one of the following diagnoses: infectious syphilis, gonorrhoea, chancroid/donovanosis/LGV, chlamydia, NSU, trichomoniasis, scabies/pediculosis, HSV/HPV first attack or molluscum contagiosum. §Through unlinked anonymous testing of neonatal dried blood spots.) Data source: Unlinked Anonymous Programme.
However, the recent increases in reports of new HIV diagnoses have largely been driven by heterosexually acquired infections, which accounted for 57% (3152/5542) of all those reported in 2002. Of these infections, three quarters (2338/3152) were probably acquired in Africa (table 1). Estimates of the total prevalent infections indicate that by the end of 2002, 15 400 African heterosexuals aged over 15 were living with HIV in the United Kingdom, of whom 4800 (31%) were undiagnosed.
View this table: [in this window] [in a new window] Table 1 Subcategory of HIV infections diagnosed in the United Kingdom that were probably acquired heterosexually, 19922002 In 2002, one third (1850/5542) of new HIV diagnoses were probably acquired in the United Kingdom. Although 80% (1500) of these infections were diagnosed in homo/bisexual men, since 1997 there has been a steady increase in the number of diagnoses of heterosexually acquired HIV infection in the United Kingdom. In 2002, 275 such HIV infections were diagnosed compared to 141 in 1997 (table 1); 56% (153/275) of these diagnoses were acquired through partners who were probably infected outside Europe. In England, Wales, and Northern Ireland, although remaining low, the prevalence of previously undiagnosed HIV infection rose significantly among UK born heterosexual males from 0.12% (30/24 465) to 0.3% (72/24 040) between 1997 and 2002 (p<0.0001); prevalence in UK born women was unchanged.
Major acute STI diagnoses reported through KC60 returns have continued their rising trend since the mid-1990s. From 1997 to 2002, there was a 103% increase to 82 206 chlamydia diagnoses (rates were 138/100 000 in males and 167/100 000 in females); a 97% increase to 24 958 gonorrhoea diagnoses (males: 66/100 000, females: 167/100 000); a 716% increase to 1232 syphilis diagnoses (males: 4/100 000, females: 0.5/100 000); a 9% increase to 69 449 genital warts diagnoses (males: 141/100 000, females: 118/100 000); and a 17% increase to 18 379 genital herpes diagnoses (males: 26/100 000, females: 42/100 000) in England, Wales, and Northern Ireland. Laboratory reports of STIs have also increased recently in Scotland; 12 392 chlamydia positive isolates were reported in 2002, a 16% increase on 2001 (10 636).
STIs have risen markedly among homo/bisexual men (fig 2). In this population, cases of gonorrhoea have almost doubled from 1842 in 1999 to 3363 in 2002, and cases of syphilis have increased from 52 to 607 over the same period; this latter rise is as a result of ongoing outbreaks in urban centres in the United Kingdom.22
View larger version (28K): [in this window] [in a new window] Figure 2 Trends in rates of major acute STIs in homo/bisexual men*, United Kingdom{dagger}, 19952002. (*Rates are based on an estimated population of 310 000 homo/bisexual men resident in England, Wales, and Scotland.25 {dagger}2001 and 2002 data not available for Scotland for KC60 and ISD(D)5 data.) Data sources: KC60 statutory returns and ISD(D)5 data, and HIV/AIDS Reports, reports received by the end of June 2003.
Among heterosexuals, young people and black minority communities continue to be disproportionately represented in STI statistics. Rates of diagnoses of chlamydia in GUM clinics have increased by 215% in women aged 1624, from 529/100 000 in 1997 to 1135/100 000 in 2002 in England, Wales, and Northern Ireland (fig 3). In the 2002 GRASP data collection, black ethnic groups, mainly black Caribbeans, accounted for 55% (516/936) and 44% (249/563) of gonococcal isolates collected from heterosexual males and females respectively (fig 4).
View larger version (22K): [in this window] [in a new window] Figure 3 Trends in the rates of selected acute STIs in young females and males aged 1624 in the United Kingdom*, 19952002. (A) Males. (B) Females. (*2001 and 2002 data not available for Scotland.) Data source: KC60 Statutory returns and ISD(D)5 data.
View larger version (17K): [in this window] [in a new window] Figure 4 Proportion of new diagnoses of uncomplicated gonorrhoea by ethnicity, England and Wales, 2002. Data source: Gonococcal Resistance to Antimicrobials Surveillance Programme (GRASP).
POPULATION SUBGROUPS Homo/bisexual men Since HIV/AIDS reporting began in the United Kingdom in the early 1980s there have been 29 890 HIV diagnoses reported in homo/bisexual men, 12 284 of whom have progressed to AIDS, and 8761 of whom have died. HIV was the third most commonly diagnosed major STI in homo/bisexual men in 2002 (fig 2).
In 2002, the UA GUM survey found that 6.5% (97/1495) of previously undiagnosed HIV infected homo/bisexual men were co-infected with an acute STI; the equivalent figure in Scotland was 2.9% (12/416) and elsewhere in England, Wales, and Northern Ireland, 3.5% (25/719). Such individuals are of particular concern since they may be at higher risk of passing on their HIV infection to others. In London, 4% (27/672) of homo/bisexual men under 25 years attending GUM clinics had a previously undiagnosed HIV infection a clear indication of continuing HIV transmission at relatively high levels. Application of STARHS found that annual HIV incidence among homo/bisexual men rose to approximately 3.5% in 2002,26 compared to 23% from 19952001,27 although this difference is not statistically significant. The highest incidence was seen in those aged 3544 (5.9%, 95% confidence intervals 3.7 to 8.8). This increasing trend occurred in a period when there were intensive health promotion campaigns and when 6070% of diagnosed HIV infected homo/bisexual men were on antiretroviral therapy (ARV).
Since 1999, considerable increases in the rate of acute STI diagnoses in homo/bisexual men attending GUM clinics have been observed (fig 2). Rates of gonorrhoea diagnoses doubled between 1999 and 2001, from 612/100 000 to 1242/100 000. A slight decrease was observed overall in 2002, but there was no decrease in men aged 1624 where rates increased from 648/100 000 in 1999 to 1194/100 000 in 2002. In 2002, rates of homosexually acquired infectious syphilis have shown a marked rise since 1999 (616%). This has been associated with a series of large localised outbreaks in Brighton, Manchester, Newcastle upon Tyne, London,22 central Scotland,28 and Northern Ireland.29 Data collected between April 2001 and September 2003 from the ESS programme indicate that 46% of homo/bisexual men diagnosed with infectious syphilis in London were co-infected with HIV. Increases in genital chlamydia infections in homo/bisexual men were also observed in 2002, up 144% since 1999.
Factors influencing transmission Behavioural surveillance data among homo/bisexual men in the United Kingdom have demonstrated increases in rates of unprotected anal intercourse (UAI), and specifically, UAI involving HIV discordant or unknown status partners.30 Data from Natsal 200025 suggest that there have been increases in the prevalence of male homosexual behaviour in the general population, and increases in some high risk behaviours among homosexually active men.31 The reasons for this rising risk are unclear. However, continued liberalisation of attitudes towards homosexuality,32 and "safer sex" fatigue in the era of ARV,33 coupled with expansions in opportunities which facilitate partner acquisition (for example, the internet, saunas)34 may be contributing factors.
Young people People aged 1624 accounted for just over 10% (588/5542) of all reports of new HIV diagnoses in 2002; a proportion that has remained constant over time. Their risk exposure distribution was similar to that of people aged over 24. Heterosexual HIV acquisition accounted for 63% (370/588) of new HIV diagnoses in 2002 in those aged 1624, with the majority of individuals (65%, 242/370) probably infected in Africa.
Rates of STIs have risen markedly among young people (fig 3) and this population subgroup bear a disproportionate burden of STI diagnoses. In 2002, women aged 1624 accounted for 72% (33 205/46 140) of all female chlamydia diagnoses, 66% (5031/7569) of gonorrhoea, 62% (50/137) of syphilis and 61% (19 792/32 544) of genital warts reported from GUM clinics in England, Wales, and Northern Ireland.
Rates of diagnoses from GUM clinics for chlamydia, gonorrhoea, and genital warts were highest among females aged 1619 and males aged 2024. The highest rates of chlamydial diagnoses were seen in women aged 1619 and men aged 2024 at 1209 and 842/100 000 respectively. These figures are likely to underestimate the total number of infections because most infections in women are asymptomatic, and thus care and treatment are not sought. Chlamydial infections diagnosed in primary care and other community settings13 are not reported in the KC60 returns and also contribute to this underestimation. Of women diagnosed with gonorrhoea, 40% were under 20. In men, rates of gonorrhoea were highest in those aged 2024 in 2002 (296/100 000), an increase of 231% since 1997. Similarly, rates of genital herpes simplex infection remain highest among males and females aged 2024 (93/100 000 and 296/100 000 respectively). Unlike other bacterial STIs, rates of syphilis among young people remain low.
Factors influencing transmission Young people are behaviourally more vulnerable to STI acquisition as they generally have higher numbers of sexual partners, more concurrent partnerships, and change partners more often than older age groups.35 Although consistent and proper use of condoms reduces the risk of STI transmission and unintended pregnancy, many young people may not have developed the skills and confidence to implement this successfully.36
STI re-infection is a particular concern in this population. In a study of three GUM clinics,37 young age was a key determinant of STI re-infection within a year of initial diagnosis. Studies in the United States have also found that re-infection rates are high among adolescents and young adults, particularly women,38 including those aged under 15.39
Black and ethnic minority populations The number of HIV infected black African adults born in the United Kingdom is increasing but currently remains low. It is estimated that in 2002, black African adults accounted for 63% (15 400) of the total of prevalent HIV infections in heterosexuals, and 51% (4800) of heterosexuals who are unaware of their HIV infection. In 2002, of the 12 203 HIV infected heterosexuals reported to SOPHID, 68% (8262) of those for whom ethnicity was reported were black African (a 330% increase since 1997), 4% (501) black Caribbean, and 21% (2580) white. The UA pregnant women surveys found an HIV prevalence of 2.5% (239/47 075) in women born in sub-Saharan Africa who gave birth in 2002. This compares with a prevalence of 0.03% (42/121 833) in their UK born counterparts (fig 1B). These data reflect the focus of the HIV pandemic in sub-Saharan African countries and the impact of population movement on the UK statistics.
Undiagnosed HIV infection continues to be a feature of the treatment histories of black heterosexuals. Among sub-Saharan born heterosexuals included in the UA GUM survey, the prevalence of previously undiagnosed HIV infection rose to 4.2% (159/3752) in London and 7.9% (60/757) outside London (fig 1B). The latter figure may be due to the recent dispersal to areas outside London of migrant populations originating from high HIV prevalence countries. In Scotland, the prevalence of previously undiagnosed HIV infection was 5.7% (9/157) in heterosexuals of African nationality, compared to 0.1% (13/133 314) in heterosexuals of British nationality.
STI diagnoses disproportionately fall on the United Kingdoms black minority populations.40,41 In the 2002 GRASP23 data collection (fig 4), black ethnic groups, mainly black Caribbean, accounted for 55% (516/936) and 44% (249/563) of gonococcal isolates in heterosexual males and females respectively. The ESS programme in London revealed that 48% (187/393) of heterosexual syphilis diagnoses were among black or black British ethnic groups.
Factors influencing transmission Black and ethnic minority populations in the United Kingdom continue to have poor sexual health. However, few behavioural surveys give insight into sexual health among ethnic minority groups. Variations in the burden of STIs among these populations are known to be influenced by a number of behavioural and social factors.42 Qualitative community based studies highlight variations in sexual socialisation, attitudes and community norms related to sexual behaviour; sex, religious beliefs, and degree of acculturation are all influential factors.43 Although qualitative studies suggest that variations in high risk behaviour do exist across ethnic groups,44,45 these alone cannot explain the observed disparities. Factors such as patterns of sexual mixing, differential access to curative services, and background disease prevalence in the communities concerned may also be contributing.42,46 Data from population based surveys and mathematical modelling will be needed to further elucidate these associations.
HIV SCREENING AND TREATMENT There has been some success in interventions aimed at reducing HIV transmission in the United Kingdom. Diagnosis at an earlier stage of HIV infection presents the opportunity for treatment to postpone further illness and to reduce viral load which, along with changes in sexual behaviour, may reduce the risk of onward HIV transmission.
The number of GUM clinic attendees accepting a voluntary confidential HIV test (VCT) can be measured through the UA GUM survey, which collects KC60 data in addition to limited demographic information. Voluntary confidential HIV testing (VCT) has increased in homo/bisexual men and heterosexuals respectively, from 45% (2724/6019) and 25% (16 886/66 880) in 1997, to 62% (4604/7372) and 54% (40 746/74 935) in 2002 in England, Wales, and Northern Ireland. From 2003, modified KC60 data will allow better monitoring of VCT uptake. In Scotland, data indicate that uptake of VCT has increased in homo/bisexual men and heterosexuals respectively, from 47% (454/959) and 23% (2624/11 223) in 1997, to 59% (761/1290) and 36% (5142/14 281) in 2002.
Similarly, over recent years, CD4 surveillance data show a recent trend towards earlier diagnosis for homo/bisexual men. Only 24% of homo/bisexual men had a CD4 cell count less than 200 cells x106/l at HIV diagnosis (an indicator of a "late diagnosis") in 2002 compared to 28% in 1997. In contrast, 43% of newly diagnosed heterosexuals had a "late diagnosis" in 2002. This may be because a high proportion of heterosexuals were infected, and previously lived abroad. Additionally, heterosexuals may perceive themselves to be at lower risk from HIV and may present for testing only when they become symptomatic.47,48
In England, the proportion of HIV infected pregnant women remaining undiagnosed by the time of delivery has declined since the introduction of the universal offer and recommendation of an HIV test as a routine part of antenatal care in 199949,50; this policy has now been introduced elsewhere in the United Kingdom.
In 2002 there were an estimated 686 births to HIV positive women in England, Wales and Scotland, of whom at least 79% (539/686) were reported as diagnosed before delivery. Overall, HIV detection rates in 2002 are currently estimated at 75% (318/422) for London, 85% (199/234) elsewhere in England and Wales and 73% (22/30) in Scotland (fig 5). These minimum estimates are subject to reporting delay and are likely to rise as more diagnosed infections in pregnancies are reported.
View larger version (29K): [in this window] [in a new window] Figure 5 Estimated proportion of HIV infected women diagnosed before delivery* and of exposed children becoming infected with HIV{dagger}{ddagger}, 19972002. (A) London. (B) Outside LondonEngland, Wales, and Scotland. (*Includes those previously diagnosed and those diagnosed through antenatal testing. {dagger}Assumes a vertical transmission rate of 26.5% in undiagnosed women and 2.2% in diagnosed women.53 {ddagger}These data contain reports received by the end of September 2003. §Data for 2002 should be considered preliminary minimum estimates, and as the number of reports rise, estimates of infants becoming HIV infected will fall.) Data source: Unlinked Anonymous Programme and the National Study of HIV in Pregnancy and Childhood (NSHPC).
These improved maternal HIV detection rates have reduced the proportion of exposed children who go on to acquire the infection vertically. In London, in 2002 (based on the current estimated detection rates), the estimated proportion of children exposed to HIV vertically who were themselves infected was 8% (35/422) compared with 19% (37/200) in 1997. In the rest of the United Kingdom this proportion decreased from 22% (25/113) in 1997 to 6% (16/264) in 2002.
A high proportion of HIV infected people who were eligible for ARV were on medication in 2002 in the United Kingdom. Of the 1708 homo/bisexual men with CD4 counts of 200 cells x106/l or less, 78% were on therapy; of the 2433 heterosexuals, 78% were on therapy; and of the 211 IDUs, 73% were on therapy (measured through SOPHID). Equivalent figures were higher for Scotland: 92% (72, p = 0.006), 94% (84, p = 0.0004), and 92% (98, p = 0.0002). However, in Scotland ARV therapy is measured through CD4 monitoring which is largely undertaken to assess a patients eligibility for ARV. These data confirm that exposure group does not affect the level of therapy uptake.
DISCUSSION The surveillance data confirm that HIV and other STIs have increased within the UK population. Population subgroups that have high rates of sexual partner change continue to have higher infection rates, in particular HIV and STIs among homo/bisexual men and STIs among young people. Black and ethnic minority populations (including subgroups born in high prevalence countries) are disproportionately affected by poor sexual health. There is some evidence of onward HIV transmission rising within the United Kingdom though as yet this is limited.
Health promotion campaigns, targeted HIV and chlamydia screening initiatives, and increased sensitivity of diagnostic tests may all have played a part in the rising number of HIV and STI diagnoses reported in 2002. The well documented pressure mounting upon GUM clinics3 through increased numbers of high risk patients attending has undoubtedly contributed to the observed trends. Since KC60 returns data are aggregate, it is not possible to determine what proportion of attendees are re-attending for follow up and/or are becoming re-infected. A disaggregate STI surveillance system is currently under development and will help interpretation of future trends.
STI diagnoses are mainly reported through GUM clinics and voluntarily from NHS laboratories. The former misses cases diagnosed in other settings and the latter reports are incomplete. This combined with the requirement for data accuracy over data quantity may have led to a general underestimate of HIV and STI diagnoses in the United Kingdom.
Indications from Natsal 200025 of increasing high risk behaviour (including concurrent partnerships and higher rates of partner acquisition), the continuing immigration of heterosexuals from countries of high HIV prevalence, and the suggested rising of HIV incidence, undiagnosed HIV infection, and STI diagnoses in homo/bisexual men all indicate that sexual health is deteriorating and the documented increases are real.
Through national collaboration, high levels of data reporting, analysis and feedback performed in conjunction within a complementary set of UK surveillance systems, allow the data to be used as a powerful tool in providing information for action. The role of surveillance has been instrumental in the creation and monitoring of successful initiatives such as the introduction of the universal offer and recommendation of an HIV test in pregnant women.49,50
Our data confirm the need for national and local prioritisation of sexual health and HIV prevention activities. Interventions such as those outlined in the English Sexual Health and HIV Strategy4 need to be implemented urgently. For homo/bisexual men this includes HIV/STI education, promotion of safer sex and HIV testing, and increasing the uptake of hepatitis B vaccination in GUM clinics. The strategy has also specifically identified young people as a priority group for action and the Department of Health is currently implementing a range of interventions including the National Chlamydia Screening Programme. The persistent ethnic disparities in sexual health outcomes deserve even greater attention, particularly with emerging evidence of increasing HIV transmission within the United Kingdom among black communities. The disaggregate STI surveillance system currently under development51 will allow ethnic disparities in sexual health to be monitored in the future and will facilitate the determination of where preventive efforts need to be targeted. In the meantime, key interventions for prioritisation include improving access to treatment and care services in hyperendemic areas; raising community HIV/STI awareness; and enhancing secondary prevention actives including partner notification.42
Key messages
* Prevalence of HIV infection in the United Kingdom is increasing; an estimated 49 500 adults aged over 15 were living with HIV in the United Kingdom in 2002, of whom 31% were unaware of their infection * While many newly diagnosed heterosexual cases are thought to have acquired their infection overseas, there is evidence of continuing transmission of HIV in the United Kingdom, particularly among homo/bisexual men * New diagnoses of major acute STIs have risen in the past 5 years, with rates highest in homo/bisexual men and young people * Effective surveillance is essential to provide timely information on the changing epidemiology of HIV and other STIs in the United Kingdom
Elsewhere in the United Kingdom, health promotion campaigns aimed at high risk subgroups are being implemented and will undoubtedly require scaling up in the near future. In Wales, for example, the "Come Clean" multimedia campaign has been run by BBC Wales and the Welsh Assembly and is targeted at young people.52 Effective secondary prevention activities are also needed to tackle the growing problem of STI re-infection and epidemiological synergy between STIs and HIV infection. Such initiatives need to be fully supported and sustained if further deterioration in the United Kingdoms sexual health is to be prevented. Finally, although the impact of these initiatives can only be recognised over many years it is important that medium and long term targets are set and progress monitored to ensure the most appropriate, cost effective, and efficient use of scarce resources.
Further information on HIV/STI surveillance trends can be found in a report published by the Health Protection Agency and others: Health Protection Agency, SCIEH, ISD, National Public Health Service for Wales, CDSC Northern Ireland and the UASSG. Renewing the focus. HIV and other Sexually Transmitted Infections in the United Kingdom in 2002. London: Health Protection Agency November 200312 (www.hpa.org.uk/infections/topics_az/hiv_and_sti/publications/annual2003/annual20 03.pdf).
ACKNOWLEDGEMENTS We extend our thanks to everybody who contributed to the writing of the annual report: Renewing the Focus: Tim Chadborn, Glenn Codere, Leah de Souza, Sarah Dougan, Gillian Elam, Josh Forde, John Harris, Vivian Hope, Alisha Johnston, Louise Logan, Catherine Lowndes, Neil MacDonald, Helen Munro, Bela Patel, Lara Payne, Brian Rice, Elizabeth Rudd, Ian Simms, and Katy Sinka.
We gratefully acknowledge the continuing collaboration of the Sexually Transmitted and Blood Borne Viruses Laboratory, Specialist and Reference Microbiology Division, Health Protection Agency, and of clinicians, microbiologists, immunologists, public health practitioners, occupational health doctors and nurses, and other colleagues who contribute to the surveillance of HIV and STIs in the United Kingdom.
We would like to thank our collaborating centres for HIV and AIDS surveillance in the UK: The Scottish Centre for Infection and Environmental Health; The Institute of Child Health (London); The UK Haemophilia Centres Doctors Organisation; members of the Scottish ISD(D)5 Collaborative Group; Collaborators on the Unlinked Anonymous Programme (a full list of collaborators available at www.hpa.org.uk/infections/topics_az/hiv_and_sti/hiv/epidemiology/ua.htm).
Finally, we thank Philip Mortimer for commenting on this paper and we are also grateful to colleagues at the UK Departments of Health both for funding specific surveys and for helpful comments on this paper at draft stage.
CONTRIBUTORS AB, ST with KS, CM, SLM, and GM, analysed the data from the Unlinked Anonymous Surveys, HIV/AIDS reports, prevalence estimates and behavioural surveillance, STI surveillance, and STARHS respectively with support from BG, NG, FN, and KF; DG, DT, and BS analysed and are responsible for data from the Scottish Centre Infection and Environmental Health, the National Public Health Service for Wales, CDSC, and the Health Protection Agency, CDSC, Northern Ireland respectively; PT coordinates the National Study of HIV in Pregnancy and Childhood and collaborated with the analysis of the Unlinked Anonymous Pregnant Women Surveys; NG is the programme manager and is responsible for data from the Unlinked Anonymous Programme; BG is responsible for data from HIV/AIDS reports; and FN is responsible for data from the unlinked anonymous surveys of Pregnant Women. JP is responsible for laboratory aspects for the Unlinked Anonymous Surveys and assisted with the interpretation of data; all authors were involved in interpretation of the results and drafting the paper; AB undertook the main writing of the paper.
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Sexual behaviour in women attending a genitourinary medicine clinic. 1988. Sex Transm Infect 2000;76(Suppl 1):S41.[Medline] 45. Evans BA, Bond RA, MacRae KD. Sexual behaviour and sexually transmitted infection among African and Caribbean men in London. Int J STD AIDS 1999;10:7448.[CrossRef][Medline] 46. Low N, Connell P, McKevitt C, et al. "You cant tell by looking": pilot study of a community-based intervention to detect asymptomatic infections. Int J STD AIDS 2003;14:8304.[CrossRef][Medline] 47. Burns FM, Fakoya AO, Copas AJ, et al. Africans in London continue to present with advanced HIV disease in the era of highly active antiretroviral therapy. AIDS 2001;15:24535.[CrossRef][Medline] 48. Del Amo J, Petruckevitch A, Phillips AN, et al. Disease progression and survival in HIV-1 infected Africans in London. AIDS 1998;12:12039.[CrossRef][Medline] 49. Department of Health. Targets aimed at reducing the number of children born with HIV: report from an expert group. 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Related Article
Surveillance: information for action H Ward Sex. Transm. Inf. 2004 80: 158. [Extract] [Full Text]
Death - 14 Oct 2005 23:47 GMT "GMCarter" <fiar@verizon.net> wrote in message
> http://sti.bmjjournals.com/cgi/content/full/80/3/159 > Sex Transm Infect 2004;80:159-166 [quoted text clipped - 8 lines] > 1997 to 2002 overall; STI rates disproportionately affect > homo/bisexual men and young people. LOL, when I posted this some months ago, ah.....what were the names you called me? OH, bigot and racist.
Welcome to my world.
GMCarter - 15 Oct 2005 11:34 GMT snip...
>LOL, when I posted this some months ago, ah.....what were the names you called me? >OH, bigot and racist. LOL...I doubt you posted anything but bits that you found supportive of your bigotry and racism. You ARE a bigot and racist--you make it quite clear in all your posts.
>Welcome to my world. No--that's your karma, dear.
George M. Carter
Death - 15 Oct 2005 23:14 GMT "GMCarter" <fiar@verizon.net> wrote in message
> "Death" <Death@yourdoor.net>
> snip... > >LOL, when I posted this some months ago, ah.....what were the names you called me? > >OH, bigot and racist. > > LOL...I doubt you posted anything but bits that you found supportive > of your bigotry and racism. It was posted in toto, and I asked this question after you commented about it:
which is worse, me saying faggots spread diseases or faggots spreading the disease?
I recall you passed on the obivious answer. It would disrupt your nicely planned escape from reality.
GMCarter - 15 Oct 2005 23:30 GMT snip
>which is worse, me saying faggots spread diseases or faggots >spreading the disease? Which is worse? Me saying you're a f.cking bigot or saying you're a f.cking a.shole? I guess they're about the same.
Miss Mary Manners
Death - 16 Oct 2005 02:39 GMT "GMCarter" <fiar@verizon.net> wrote in message
> snip > >which is worse, me saying faggots spread diseases or faggots > >spreading the disease? > > Which is worse? Me saying you're a f.cking bigot or saying you're a > f.cking a.shole? I guess they're about the same. I see you passed yet again on the question coward.
GMCarter - 16 Oct 2005 11:56 GMT >"GMCarter" <fiar@verizon.net> wrote in message > [quoted text clipped - 6 lines] >> >I see you passed yet again on the question coward. I see you're still an incredibly stupid a.shole! Your question, like you, is full of sh.t and Rovian premises.
Hey--you're the one that is so terrified to sign his own name that he uses rotating sock puppets! lol...and you call me a coward?
George M. Carter
Death - 18 Oct 2005 23:56 GMT "GMCarter" <fiar@verizon.net> wrote in message
> "Death" <Death@yourdoor.net> > >> > >I see you passed yet again on the question coward. > > Hey--you're the one that is so terrified to sign his own name that he > uses rotating sock puppets! lol...and you call me a coward? Coward and a liar. I have NEVER used a sock to state my views. And you passed again on the question.
GMCarter - 19 Oct 2005 11:24 GMT >Coward and a liar. I have NEVER used a sock to state my views. >And you passed again on the question. Hahahahahahahahahahahahahahaha! Your question, like you, is full of sh.t.
Death - 19 Oct 2005 17:48 GMT "GMCarter" <fiar@verizon.net> wrote in message
> "Death" <Death@yourdoor.net> > wrote: [quoted text clipped - 3 lines] > > Hahahahahahahahahahahahahahaha! Take a tums, it helps with those gas pains.
> Your question, like you, is full of sh.t. Cowardly response. You gladly spew your vile any other time when and if it suits your agenda. An honest answer to the question would expose you for the liar and coward you have been, are, and will continue to be.
GMCarter - 19 Oct 2005 22:35 GMT snip
>Cowardly response. You gladly spew your vile any other time >when and if it suits your agenda. LOL. Coming from a homophobic racist like you, I can only giggle at you calling anyone else's commentary "vile."
George M. Carter
Death - 20 Oct 2005 01:51 GMT "GMCarter" <fiar@verizon.net> wrote in message
> "Death" <Death@yourdoor.net> > [quoted text clipped - 3 lines] > LOL. Coming from a homophobic racist like you, I can only giggle at > you calling anyone else's commentary "vile." Correct, all you can do is giggle. You surly don't have the balls to answer the question.
GMCarter - 20 Oct 2005 03:45 GMT >Correct, all you can do is giggle. >You surly don't have the balls to answer the question. Don't call me Surley. What was the question?
Death - 20 Oct 2005 20:36 GMT "GMCarter" <fiar@verizon.net>
> "Death" <Death@yourdoor.net> > > >Correct, all you can do is giggle. > >You surly don't have the balls to answer the question. > > Don't call me Surley. What was the question? Surely you remember.
Brian Mailman - 16 Oct 2005 18:15 GMT > snip >>which is worse, me saying faggots spread diseases or faggots >>spreading the disease? > > Which is worse? Me saying you're a f.cking bigot or saying you're a > f.cking a.shole? I guess they're about the same. Not at all. The latter can be useful.
B/
GMCarter - 16 Oct 2005 18:30 GMT >> snip >>>which is worse, me saying faggots spread diseases or faggots [quoted text clipped - 4 lines] > >Not at all. The latter can be useful. LOL...point well taken. So to speak.
Death - 19 Oct 2005 00:06 GMT "Brian Mailman" <bmailman@sfo.invalid> wrote in message
> > Which is worse? Me saying you're a f.cking bigot or saying you're a > > f.cking a.shole? I guess they're about the same. > > Not at all. The latter can be useful. LOL, as you've shown, it can be used as a brain, dinner plate and an aids spreader.
Isn't it hilarious that an a.shole spreads aids ? Playing in sh.t, how filthy.
Gee, I wonder why you can't find much sympathy among people who understood that the a.shole is an exit for sh.t.
Brian Mailman - 19 Oct 2005 01:34 GMT (snip self-hatred)
wow, nothing left.
B/
Death - 19 Oct 2005 02:39 GMT "Brian Mailman" <bmailman@sfo.invalid>
and you got the message
Fondoo - 22 Oct 2005 12:02 GMT Death wrote:
(snip self-hatred)
wow, nothing left.
B/
awww poor Death. Probly all the pimples and the whole "lack of pubes" thing has him down
copi - 15 Oct 2005 17:37 GMT > "GMCarter" <fiar@verizon.net> wrote in message > > [quoted text clipped - 15 lines] > > Welcome to my world. there is an interesting connection from actionlyme.org
HIV-CCR5 has to do with Treponema lipoprotein:
http://web.archive.org/web/20041013131900/http://grad.uchc.edu/phdfaculty/radolf.html
GMCarter - 15 Oct 2005 22:36 GMT >there is an interesting connection from actionlyme.org > >HIV-CCR5 has to do with Treponema lipoprotein: > >http://web.archive.org/web/20041013131900/http://grad.uchc.edu/phdfaculty/radolf.html Interesting. Utterly unsupportive of the notion that HIV and syphilis are the same disease.
To the contrary, the author points out that syphilis infection can augment infection by HIV. Not exactly news.
"Equally important, we have found that immune cell activation by T. pallidum lipoproteins enhances their expression of CCR5, an HIV co-receptor, as well as their susceptibility to HIV-1 infection, suggesting a possible mechanism for the epidemiological observation that genital ulcer diseases such as syphilis augment sexual transmission of the AIDS virus."
George M. Carter
Death - 15 Oct 2005 23:21 GMT "copi" <jerome007@arcor.de> wrote in message >
> http://web.archive.org/web/20041013131900/http://grad.uchc.edu/phdfaculty/radolf.html Good article. Here it is:
Justin D. Radolf Professor of Medicine and Center for Microbial Pathogenesis jradolf@up.uchc.edu
M.D. University of California, San Francisco Immunology Graduate Program Skeletal, Craniofacial & Oral Biology Graduate Program Genetics and Developmental Biology Graduate Program Venereal syphilis and Lyme disease are the two most prevalent spirochetal infections in the United States. These disorders share a number of clinical features and their respective etiologic agents, Treponema pallidum and Borrelia burgdorferi, share common parasitic strategies. The objective of our research is to elucidate these processes at the cellular and the molecular levels.
T. pallidum and B. burgdorferi have poorly understood abilities to persist for prolonged periods within syphilis and Lyme disease patients despite vigorous immune responses. Ultrastructural, biochemical and molecular analysis of the outer membranes of these organisms have provided significant insights into their immunological evasiveness. Compared to gram-negative bacteria (e.g., E. coli), the outer membranes of both T. pallidum and B. burgdoferi contain low densities of membrane-spanning proteins which provoke little to no host antibody response. In contrast to T. pallidum, B. burgdorferi does possess surface-exposed lipoproteins. The Lyme disease spirochete's strategy for immune evasion also seems to depend upon alteration of surface antigen composition. Several years ago, we discovered that T. pallidum and B. burgdorferi both contain large numbers of lipid-modified integral membrane proteins (i.e., lipoproteins). The covalently bound lipid moieties appear to serve two critical functions: (1) they provide membrane anchors for the hydrophilic polypeptides; and (2) they markedly enhance the ability of these proteins to activate immune cells, particularly macrophages and endothelial cells. Using synthetic lipopeptides and mutagenized forms of the lipoproteins, we are studying the signaling pathways by which they activate immune cells. We also are studying the in vivo responses to these molecules in animal models and in human skin. In addition to providing new insights into spirochetal diseases, the results obtained thus far have broad implications for our understanding of the role of the innate immune response to diverse microbial pathogens. Equally important, we have found that immune cell activation by T. pallidum lipoproteins enhances their expression of CCR5, an HIV co-receptor, as well as their susceptibility to HIV-1 infection, suggesting a possible mechanism for the epidemiological observation that genital ulcer diseases such as syphilis augment sexual transmission of the AIDS virus.
Publications
Selected References:
Narasimhan S, Camaino MJ, Liang FT, Santiago F, Laskowski M, Philipp MT, Pachner AR, Radolf JD, Fikrig E. Borrelia burgdorferi transcriptome in the central nervous system of non-human primates. Proc Natl Acad Sci U S A. 2003 Dec 23;100(26):15953-8.
Salazar JC, Pope CD, Sellati TJ, Feder HM Jr, Kiely TG, Dardick KR, Buckman RL, Moore MW, Caimano MJ, Pope JG, Krause PJ, Radolf JD; Lyme Disease Network. Coevolution of markers of innate and adaptive immunity in skin and peripheral blood of patients with erythema migrans. J Immunol. 2003 Sep 1;171(5):2660-70. Erratum in: J Immunol. 2003 Nov 1;171(9):4934.
Krause PJ, McKay K, Gadbaw J, Christianson D, Closter L, Lepore T, Telford SR 3rd, Sikand V, Ryan R, Persing D, Radolf JD, Spielman A; Tick-Borne Infection Study Group. Increasing health burden of human babesiosis in endemic sites. Am J Trop Med Hyg. 2003 Apr;68(4):431-6.
Fouad AF, Kum KY, Clawson ML, Barry J, Abenoja C, Zhu Q, Caimano M, Radolf JD. Molecular characterization of the presence of Eubacterium spp and Streptococcus spp in endodontic infections. Oral Microbiol Immunol. 2003 Aug;18(4):249-55.
Purser JE, Lawrenz MB, Caimano MJ, Howell JK, Radolf JD, Norris SJ.
A plasmid-encoded nicotinamidase (PncA) is essential for infectivity of
Borrelia burgdorferi in a mammalian host. Mol Microbiol. 2003 May;48(3):753-64.
Hazlett KR, Rusnak F, Kehres DG, Bearden SW, La Vake CJ, La Vake ME, Maguire ME, Perry RD, Radolf JD. The Treponema pallidum tro operon encodes a multiple metal transporter, a zinc-dependent transcriptional repressor, and a semi-autonomously expressed
phosphoglycerate mutase. J Biol Chem. 2003 Jun 6;278(23):20687-94.
Parveen N, Caimano M, Radolf JD, Leong JM. Adaptation of the Lyme disease spirochaete to the mammalian host environment results in enhanced glycosaminoglycan and host cell binding. Mol Microbiol. 2003 Mar;47(5):1433-44.
Bugrysheva J, Dobrikova EY, Sartakova ML, Caimano MJ, Daniels TJ, Radolf JD, Godfrey HP, Cabello FC. Characterization of the stringent response and rel(Bbu) expression in Borrelia burgdorferi. J Bacteriol. 2003 Feb;185(3):957-65.
Salazar JC, Hazlett KR, Radolf JD. The immune response to infection with Treponema pallidum, the stealth pathogen. Microbes Infect. 2002 Sep;4(11):1133-40. Review.
Fouad AF, Barry J, Caimano M, Clawson M, Zhu Q, Carver R, Hazlett K, Radolf JD. PCR-based identification of bacteria associated with endodontic infections.J Clin Microbiol. 2002 Sep;40(9):3223-31.
Clawson ML, Paciorkowski N, Rajan TV, La Vake C, Pope C, La Vake M, Wikel SK, Krause PJ, Radolf JD. Cellular immunity, but not gamma interferon, is essential for resolution of Babesia microti infection in BALB/c mice.Infect Immun. 2002 Sep;70(9):5304-6.
Hazlett KR, Cox DL, Sikkink RA, Auch'ere F, Rusnak F, Radolf JD.
Contribution of neelaredoxin to oxygen tolerance by Treponema pallidum. Methods Enzymol. 2002;353:140-56.
Eggers CH, Caimano MJ, Clawson ML, Miller WG, Samuels DS, Radolf JD. Identification of loci critical for replication and compatibility of a Borrelia burgdorferi cp32 plasmid and use of a cp32-based shuttle vector for the expression of fluorescent reporters in the lyme disease spirochaete. Mol Microbiol. 2002 Jan;43(2):281-95.
Krause PJ, McKay K, Thompson CA, Sikand VK, Lentz R, Lepore T, Closter L, Christianson D, Telford SR, Persing D, Radolf JD, Spielman A; Deer-Associated Infection Study Group. Disease-specific diagnosis of coinfecting tickborne zoonoses: babesiosis, human granulocytic ehrlichiosis, and Lyme disease. Clin Infect Dis. 2002 May 1;34(9):1184-91.
Lee YH, Dorwart MR, Hazlett KR, Deka RK, Norgard MV, Radolf JD, Hasemann CA. The crystal structure of Zn(II)-free Treponema pallidum TroA, a periplasmic metal-binding protein, reveals a closed conformation. J Bacteriol. 2002 Apr;184(8):2300-4.
Elias AF, Stewart PE, Grimm D, Caimano MJ, Eggers CH, Tilly K, Bono JL, Akins DR, Radolf JD, Schwan TG, Rosa P. Clonal polymorphism of Borrelia burgdorferi strain B31 MI: implications for mutagenesis in an infectious strain background. Infect Immun. 2002 Apr;70(4):2139-50.
copi - 15 Oct 2005 19:16 GMT New diagnoses of syphilis have increased
> eightfold doesnt that sound pretty much? time to get ccr5-inhibitors?
GMCarter - 15 Oct 2005 22:36 GMT >New diagnoses of syphilis have increased >> eightfold > >doesnt that sound pretty much? >time to get ccr5-inhibitors? They're in the works actually. Though I do not have a whole heck of a lot of faith in them. Big worry is if they push HIV to target X4, which would not be a nice thing.
George M. Carter
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