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Publication
Featured researches published by Thanyanan Chaowanachan.
Sexually Transmitted Diseases | 2008
Peter H. Kilmarx; Kelly Blanchard; Supaporn Chaikummao; Barbara Friedland; Nucharee Srivirojana; Cathy Connolly; Paisit Witwatwongwana; Somsak Supawitkul; Philip A. Mock; Thanyanan Chaowanachan; Jordan W. Tappero
Objectives: To determine the safety and acceptability of use of Carraguard, a carrageenan-derived candidate microbicide gel, during sexual intercourse in women and men. Study Design: We conducted a 6-month randomized, placebo-controlled trial among sexually active, couples at relatively lower risk for HIV infection in northern Thailand. Methods: Women inserted 1 applicator of study gel vaginally every time the couple had sex. Safety was assessed by symptom report and genital examination of both partners and by changes in vaginal flora. Acceptability was assessed by participant interview. Results: Overall, 55 couples were randomized, 28 to Carraguard use and 27 to the methyl-cellulose placebo gel group. Retention and study gel use were similarly high in both study groups; use of gel without condoms was reported in more than 95% of vaginal sex acts. The 2 study groups were similar in the proportions of women and men with symptoms or with genital findings without epithelial disruption, of men with findings with epithelial disruption, and of women with abnormal genital flora, whereas more women in the placebo group had findings with epithelial disruption. Women and men in both groups reported that the gel and applicator were acceptable. Conclusions: Carraguard can safely be used an average of 2 to 3 times per week during sex and is acceptable to Thai women and men.
Sexually Transmitted Diseases | 2006
Liesbeth J. M. Bollen; Rutt Chuachoowong; Peter H. Kilmarx; Philip A. Mock; Mary Culnane; Natapakwa Skunodom; Thanyanan Chaowanachan; Bongkoch Jetswang; Kanchana Neeyapun; Suvanna Asavapiriyanont; Anuvat Roongpisuthipong; Thomas C. Wright; Jordan W. Tappero
Background: Human immunodeficiency virus (HIV)–infected women are at increased risk for developing cervical cancer and for infection with human papillomavirus (HPV). Prophylactic vaccines targeting HPV types 16 and 18 are being evaluated for efficacy among young women. Goal: The goal was to assess the prevalence of HPV among HIV-infected pregnant women in Bangkok and to evaluate the need for prophylactic HPV vaccines studies in this population. Study Design: The study population consisted of 256 HIV-infected pregnant women who participated in a mother-to-child HIV transmission trial. Stored cervicovaginal lavage samples were tested for the presence of HPV DNA by polymerase chain reaction with PGMY09/11 primers and reverse line-blot hybridization for determination of anogenital HPV types. Results: HPV prevalence was 35.5% (91/256); high-risk HPV prevalence was 23.4% (60/256). HPV type 16 or 18 was present in 8.2% (21/256). Almost half of all infections were multiple. Furthermore, overall HPV detection was associated with abnormal cervical cytology (P <0.001) and higher HIV-plasma viral load (P = 0.007). Conclusions: Only one-quarter of HIV-infected pregnant women in Bangkok had high-risk HPV types; less than 10% had HPV types 16 or 18. As the HPV prevalence is expected to increase during HIV disease, prophylactic vaccines targeting HPV types 16 and 18 should be studied among HIV-infected women not yet infected with these HPV types and not previously exposed.
Clinical and Vaccine Immunology | 2005
Kovit Pattanapanyasat; Surada Lerdwana; Egarit Noulsri; Thanyanan Chaowanachan; Punneeporn Wasinrapee; Natthaga Sakulploy; Vallerut Pobkeeree; Orapin Suksripanich; Sombat Thanprasertsuk; Thomas J. Spira; Jordan W. Tappero; William C. Levine
ABSTRACT Use of the standard dual-platform flow cytometric method for determination of CD4+ T-lymphocyte counts, which needs both a flow cytometer (FCM) and hematological analyzer, would inevitably lead to increased variability. The development of new single-platform (SP) FCMs that provide direct CD4+ T-lymphocyte counts for improved assay precision and accuracy have recently attracted attention. This study evaluated one of those systems, CyFlowgreen (Partec), a single-parameter SP volumetric FCM. The performance of CyFlowgreen was compared with those of two reference standard SP microbead-based technologies of the three-color TruCOUNT tube with the FACScan FCM and a two-color FACSCount system (Becton Dickinson Biosciences). Absolute CD4+ and CD8+ T-lymphocyte counts in 200 human immunodeficiency virus type 1-seropositive blood specimens were determined. Statistical analysis for correlation and agreement were performed. A high correlation of absolute CD4 counts was shown when those obtained with CyFlowgreen were compared with those obtained with the bead-based three-color TruCOUNT system (R2 = 0.96; mean bias, −69.1 cells/μl; 95% confidence interval [CI], −225.7 to +87.5 cells/μl) and the FACSCount system (R2 = 0.97; mean bias, −40.0 cells/μl; 95% CI, −165.1 to +85.1 cells/μl). The correlation of the CD4+ T-lymphocyte counts obtained by the two bead-based systems was high (R2 = 0.98). Interestingly, CyFlowgreen yielded CD4+ T-lymphocyte counts that were 21.8 and 7.2 cells/μl lower than those obtained with the TruCOUNT and the FACSCount systems, respectively, when CD4+ T-lymphocyte counts were <250 CD4+ T-lymphocyte counts/μl range or 17.3 and 5.8 cells/μl less, respectively, when CD4+ T-lymphocyte counts were <200 cells/μl. The single-parameter CyFlowgreen volumetric technology performed well in comparison with the performance of the standard SP bead-based FCM system. However, a multicenter comparative study is needed before this FCM machine is implemented in resource-limited settings.
Journal of Acquired Immune Deficiency Syndromes | 2003
Alice Liu; Peter H. Kilmarx; Somsak Supawitkul; Thanyanan Chaowanachan; Somboonsak Yanpaisarn; Supaporn Chaikummao; Khanchit Limpakarnjanarat
Although use of rapid HIV antibody tests of finger-stick blood specimens could expand voluntary counseling and testing in areas where fear of venipuncture and delays in learning test results are barriers, there is little information on performance and acceptability of these tests in Asia. We used the Hema. Strip HIV-1/2 test (Saliva Diagnostic Systems, Vancouver, WA) in a prospective cohort study of HIV seroincidence among women in northern Thailand from 1998 to 1999. Nurses obtained whole-blood specimens by finger-stick testing and provided test results and counseling at each visit. Acceptability of the rapid test was assessed at the first 6-month follow-up visit. HIV-1 seroprevalence among the 804 women screened at enrollment was 3.1%. Positive rapid test results from 25 women were confirmed by enzyme immunoassay and Western blot analysis using serum obtained by venipuncture. Of the 741 women who returned for follow-up, 56% preferred specimen collection by finger-stick testing to venipuncture, 80% preferred immediate rather than delayed test results, 79% preferred the rapid test method to typical testing methods, and 97% were satisfied with the test method used. Results from this study demonstrate the utility and acceptability of the rapid finger-stick test for HIV antibody among women in northern Thailand.
Sexually Transmitted Diseases | 2003
Gabriela Paz-Bailey; Peter H. Kilmarx; Somsak Supawitkul; Thanyanan Chaowanachan; Supaporn Jeeyapant; Maya Sternberg; Lauri E. Markowitz; Timothy D. Mastro; Frits van Griensven
Background Previous studies of sexual behavior and sexually transmitted diseases (STDs) in Thai adolescents may have been limited by participation bias and underreporting of stigmatized behaviors. Goal The goal was to increase knowledge about risk behaviors and STDs among youths in Thailand. Study Design Students aged 15 to 21 years completed an audio-computer-assisted self-interview. Oral fluid was tested for HIV antibodies and urine was tested for Chlamydia trachomatis and Neisseria gonorrhoeae nucleic acids with polymerase chain reaction. Results Of 1736 invited students, 1725 (99.4%) agreed to participate. Overall, C trachomatis infection was detected in 49 (2.8%), and there were five cases (0.3%) each of infection with N gonorrhoeae and HIV. Among those who reported sexual intercourse, the prevalence of chlamydial infection was 3.7% among men and 6.1% among women. Logistic regression analysis showed age-adjusted factors associated with chlamydial infection among men to be parents’ occupation in agriculture, having sold sex, having a sex partner who had been pregnant, and the number of casual sex partners during lifetime. Among women, age-adjusted factors were parents’ occupation in agriculture, number of casual partners during lifetime, having an older sex partner, and perception of higher HIV infection risk. Conclusion These adolescents had high rates of unprotected intercourse and are at risk for STDs. Prevention programs should emphasize use of effective contraceptive methods, including condom use; reducing the number of sex partners (stressing the risk a partner of older age may pose to female adolescents); and reducing engagement in commercial sex.
Journal of Acquired Immune Deficiency Syndromes | 2004
Lily Nguyen; Thanyanan Chaowanachan; Suphak Vanichseni; Janet M. McNicholl; Philip A. Mock; Robert Nelson; Thomas W. Hodge; Frits van Griensven; Kachit Choopanya; Timothy D. Mastro; Jordan W. Tappero; Dale J. Hu
The loss of viral control by the host may be due to the evolution of viruses with mutations that limit presentation by human leukocyte antigen (HLA) to cytotoxic T cells. The authors hypothesized that the consequence of such evolution might be that persons with common HLA class I alleles would be less able to control viremia, on average, than would those with rare alleles. HLA class I typing was completed for 128 injection drug users who seroconverted in a prospective cohort study in Bangkok, Thailand. Logistic regression was used to model viral load (greater than or equal to the median) at 9 and 12 months after seroconversion with an HLA score that profiled the relative prevalence of each individual’s alleles. At 12 months after seroconversion, injection drug users with the most common HLA alleles (highest quartile HLA score) had an almost 4-fold increased risk for higher viral load (≥32,055 copies/mL) than injection drug users with less common HLA alleles (adjusted odds ratio, 3.92; 95% confidence interval, 1.3–11.8). These findings support the importance of frequency-dependent effects of host genes on HIV type 1 evolution in different populations and suggest that HLA-driven viral evolution critically influences control of viremia in early HIV type 1 infection.
Journal of Acquired Immune Deficiency Syndromes | 2004
Kate Buchacz; Dale J. Hu; Suphak Vanichseni; Philip A. Mock; Thanyanan Chaowanachan; La-ong Srisuwanvilai; Roman Gvetadze; Frits van Griensven; Jordan W. Tappero; Dwip Kitayaporn; Jaranit Kaewkungwal; Kachit Choopanya; Timothy D. Mastro
Background: Some candidate HIV-1 vaccines may not prevent HIV-1 infection but may alter the course of disease. Surrogate endpoints based on early laboratory makers in HIV-1–infected persons who are antiretroviral therapy (ART)–naive will be useful for evaluating vaccine efficacy in slowing disease progression (VEp). We examined pretreatment HIV-1 viral loads and CD4 cell counts in recent HIV-1 seroconverters to inform selection of these endpoints. Methods: We studied 130 newly HIV-1–infected injection drug users identified from a prospective cohort of initially uninfected persons in Bangkok during 1995 through 1998. We analyzed trends in HIV-1 viral loads and CD4 cell counts as well as progression to the surrogate endpoint, defined as 2 consecutive CD4 cell counts of fewer than 350 cells/mm3, during 24 months after the first HIV-1 seropositive (FP) visit. Results: Median HIV-1 RNA copies/mL with interquartile ranges were 43,693 (14,320–94,767) at the FP visit, 46,924 (16,273–104,314) at 6 months, 28,446 (11,292–54,325) at 12 months, and 18,080 (8713–54,059) at 18 months. HIV-1 viral loads at the FP visit and at 18 months were positively correlated (r = 0.53, P < 0.0001). Of 130 participants, 12% reached the surrogate endpoint by 6 months, 16% by 12 months, and 27% by 18 months. In Cox regression analyses, HIV-1 viral loads of more than 50,000 copies/mL at the FP visit (hazard ratio [HR] = 2.3, 95% confidence interval [CI]: 1.1–4.8) and first CD4 cell count of 500 or fewer cells/mm3 (HR = 7.6, 95% CI: 3.2–17.6) were independently associated with faster progression to the surrogate endpoint. Conclusions: Participants with high HIV-1 RNA levels and low CD4 cell counts close to the time of seroconversion were more likely to experience early immunologic progression. Approximately one quarter of seroconverters reached the surrogate immunologic endpoint within 18 months of their FP visit and before starting ART, suggesting the utility of this endpoint for analyses of VEp in some ongoing and planned HIV-1 vaccine efficacy trials.
Infectious Diseases in Obstetrics & Gynecology | 2008
Denise J. Jamieson; Natapakwa Skunodom; Thanyanan Chaowanachan; Anuvat Roongpisuthipong; William A. Bower; Tawee Chotpitayasunondh; Wendy Bhanich Supapol; Wendi L. Kuhnert; Wimol Siriwasin; Jeffrey Wiener; Sanay Chearskul; Michelle S. McConnell; Nathan Shaffer
Objective. The purpose of this study was to describe the epidemiology of coinfection with hepatitis C virus (HCV) and HIV among a cohort of pregnant Thai women. Methods. Samples from 1771 pregnant women enrolled in three vertical transmission of HIV studies in Bangkok, Thailand, were tested for HCV. Results. Among HIV-infected pregnant women, HCV seroprevelance was 3.8% and the active HCV infection rate was 3.0%. Among HIV-uninfected pregnant women, 0.3% were HCV-infected. Intravenous drug use by the woman was the factor most strongly associated with HCV seropositivity. Among 48 infants tested for HCV who were born to HIV/HCV coinfected women, two infants were HCV infected for an HCV transmission rate of 4.2% (95% 0.51–14.25%). Conclusions. HCV seroprevalence and perinatal transmission rates were low among this Thai cohort of HIV-infected pregnant women.
Sexually Transmitted Diseases | 2008
Sara Whitehead; Wanna Leelawiwat; Supaporn Jeeyapant; Supaporn Chaikummao; John R. Papp; Peter H. Kilmarx; Lauri E. Markowitz; Jordan W. Tappero; Thanyanan Chaowanachan; Wat Uthaivoravit; Frits van Griensven
Background: Monitoring changes in adolescent sexual risk behaviors and sexually transmitted infections is critical for evaluating the effectiveness of human immunodeficiency virus and other prevention programs, but population-based data on adolescents in Thailand are limited. We report findings from 2 cross-sectional surveys conducted in 1999 and 2002 among 15-to 21-year-old vocational students. Methods: In 1999 and 2002, 1725 and 966 students, respectively, were interviewed using computer-assisted self-interview methods. Urine samples were collected and tested for Chlamydia trachomatis and Neisseria gonorrhoeae by polymerase chain reaction. Results: From 1999 to 2002 C. trachomatis prevalence increased from 3.2% to 7.5% (P <0.001) in women and from 2.5% to 6.0% (P <0.001) in men. There was an increase in the reported mean lifetime number of steady sexual partners among both men (3.4–4.7, P = 0.01) and women (2.5–3.3, P <0.001), and in the mean lifetime number of casual partners among men (1.1–2.1, P <0.001) and women (0.3–1.1, P = 0.04). Reported consistent condom use decreased significantly among women with casual partners (43%–19%, P = 0.03) but not among men (25%–31%, P = 0.31). Conclusions: Our study identified important increases in the prevalence of chlamydial infection and in sexual risk behaviors among Thai adolescents over a 3-year period. These findings are consistent with other studies suggesting profound social changes are changing norms of adolescent sexual behavior in Thailand, and highlight the need for adolescent sexual health services and prevention programming.
Journal of Acquired Immune Deficiency Syndromes | 2012
Richard E. Haaland; Thanyanan Chaowanachan; Tammy Evans-Strickfaden; Janneke van de Wijgert; Peter H. Kilmarx; Catherine A. McLean; Clyde E. Hart
CD4 count to those previously with restricted access to such testing. Using a disposable PIMA CD4 cartridge containing sealed reagents, and the portable PIMA Analyser, the Alere PIMA CD4 test delivers an absolute count of T-helper cells from either a fingerprick or venous whole blood sample within 20 minutes as against one-and-a-half hour on the FACS count. The absolute CD4 cell count obtained using the PIMA system correlated well with those of the FACS Count, with no statistically significant difference and with low bias, for all ranges of the CD4 counts. The Alere PIMA CD4 test system was found to be a handy and portable user-friendly point of care and system with a performance at par with that of a conventional flow cytometer for absolute CD4 counts. Because it is battery operated, it has a potential for field applicability in high-burden resourcepoor countries. The user would find it to be an accurate and cost-effective tool in the management of HIV patients, especially in remote locations or resource limited setups.