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1. |
EditorialJAIDSat 15: Meeting the Challenge |
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JAIDS Journal of Acquired Immune Deficiency Syndromes,
Volume 32,
Issue 1,
2003,
Page 1-1
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ISSN:1525-4135
出版商:OVID
年代:2003
数据来源: OVID
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2. |
The Potential Public Health and Community Impacts of Safer Injecting Facilities: Evidence From a Cohort of Injection Drug Users |
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JAIDS Journal of Acquired Immune Deficiency Syndromes,
Volume 32,
Issue 1,
2003,
Page 2-8
Evan,
Wood Thomas,
Kerr Patricia,
Spittal Kathy,
Li Will,
Small Mark,
Tyndall Robert,
Hogg Michael,
O'Shaughnessy Martin,
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摘要:
BackgroundAlthough medically supervised safer injecting facilities (SIFs) remain untested in North America, their implementation is currently being debated. Reluctance of health policy makers to initiate a pilot study of SIFs may in part be hindered by outstanding questions regarding the potential community and public health impact of the intervention. Specifically, it is presently unknown if those at greatest risk of overdose and HIV transmission or those responsible for community impact of injection drug use will be willing to attend.MethodsThe current study was conducted to evaluate the proportion of injection drug users (IDU) willing to attend medically supervised SIFs, if they were available, among participants enrolled in the Vancouver Injection Drug User Study (VIDUS). The authors also evaluated factors associated with willingness to use a SIF using univariate and logistic regression analyses. Participants who were followed from June 2001 to June 2002 were eligible for the present analyses.ResultsOverall, 587 active IDU responded to a questionnaire during the study period. Among respondents, 215 (36.6%) expressed willingness to attend a SIF. Variables that were independently associated with willingness to attend a SIF in multivariate analyses included having difficulty accessing sterile syringes (adjusted odds ratio [AOR] = 2.07), requiring help injecting (AOR = 1.52), frequently injecting heroin (AOR = 1.81), sex trade work (AOR = 2.02), and injecting in public spaces (AOR = 2.00).ConclusionsSeveral variables that have recently been associated with overdose, syringe sharing, HIV and HCV incidence, and community impact of illicit drug use in this setting were associated with willingness to attend medically supervised SIFs. Although the impact of SIFs in North America can only be quantified by scientific evaluation, these data indicate a high potential for immediate community and public health benefits if SIFs were presently available.
ISSN:1525-4135
出版商:OVID
年代:2003
数据来源: OVID
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3. |
Comparison Between Env-Specific T-Cell Epitopic Responses in HIV-1-Uninfected Adults Immunized with Combination of ALVAC-HIV(vCP205) Plus or Minus rgp160MN/LAI-2 and HIV-1-Infected Adults |
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JAIDS Journal of Acquired Immune Deficiency Syndromes,
Volume 32,
Issue 1,
2003,
Page 9-17
Silvia,
Ratto-Kim Lawrence,
Loomis-Price Naomi,
Aronson Janelle,
Grimes Cristin,
Hill Chevelle,
Williams Raphaelle,
El Habib Deborah,
Birx Jerome,
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摘要:
In this study, we investigated the CD4+T-helper response induced by ALVAC-HIV(vCP205) ± rgp160MN/LAI-2 using a series of 15 overlapping amino acid peptides spanning the entire gp160MN/LAI-2 antigen. CD4+Env-specific T-cell lines were established from three groups of HIV-1–negative HIV vaccine recipients: vCP205 + gp160MN/LAI-2, vCP205 only, and gp160MN/LAI-2 only. CD4+Env-specific T-cell lines established from individuals who received the prime-boost vCP205 + rgp160MN/LAI-2 generated strong and broad T-helper responses scattered across the Env sequence, whereas Env-specific T-cell lines from individuals receiving the vCP205 vaccine alone generated reactivity to only a few peptides. CD4+-specific T-cell lines were also established from HIV-1–infected individuals and demonstrated poor reactogenicity to Env peptides in both breadth and amplitude of response. These results highlight the complexity of major histocompatibility complex class II presentation and CD4+antigen-specific reactivity, emphasizing the need to better understand these crucial T–helper cell responses in the setting of HIV infection and HIV vaccine development.
ISSN:1525-4135
出版商:OVID
年代:2003
数据来源: OVID
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4. |
Results of a Phase 2 Clinical Trial at 48 Weeks (AI424-007): A Dose-Ranging, Safety, and Efficacy Comparative Trial of Atazanavir at Three Doses in Combination with Didanosine and Stavudine in Antiretroviral-Naive Subjects |
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JAIDS Journal of Acquired Immune Deficiency Syndromes,
Volume 32,
Issue 1,
2003,
Page 18-29
Ian,
Sanne Peter,
Piliero Kathleen,
Squires Alexandra,
Thiry Steven,
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摘要:
Three dose levels of the protease inhibitor (PI) atazanavir (200, 400, and 500 mg once daily) were compared with nelfinavir (750 mg three times daily) when given both as monotherapy and in combination with didanosine and stavudine in 420 antiretroviral-naive subjects infected with HIV-1. Subjects received monotherapy for 2 weeks, followed by combination therapy for 46 weeks. After 48 weeks, mean change from baseline in HIV RNA (−2.57 to −2.33 log10copies/mL), the proportion of subjects with HIV RNA <400 copies/mL (56%–64%) and <50 copies/mL (28%–42%), and mean increases in CD4 cell count (185–221 cells/mm3) were comparable across treatment groups. Diarrhea was two to three times more common in the nelfinavir group (61% of subjects) than in the atazanavir groups (23%–30% of subjects,p< .0001 versus nelfinavir), and jaundice occurred only in atazanavir-treated subjects (6%, 6%, and 12% in the 200-, 400-, and 500-mg groups, respectively) (p< .03 for all atazanavir regimens vs. nelfinavir). Mean percent change from baseline in fasting low-density lipoprotein (LDL) cholesterol was significantly less in the atazanavir groups (−7% to 4%) than in the nelfinavir group (31%) (p< .0001). In conclusion, once-daily atazanavir is a potent, safe, and well tolerated PI that rapidly and durably suppresses HIV RNA and durably increases CD4 cell count in antiretroviral-naive subjects. Through 48 weeks, atazanavir was not associated with clinically relevant increases in total cholesterol, fasting LDL cholesterol, or fasting triglycerides. In comparison, nelfinavir was associated with prompt, marked, and sustained elevations in these parameters of a magnitude that suggests they are clinically relevant.
ISSN:1525-4135
出版商:OVID
年代:2003
数据来源: OVID
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5. |
The Clinical Spectrum of Hepatitis C Virus in HIV Coinfection |
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JAIDS Journal of Acquired Immune Deficiency Syndromes,
Volume 32,
Issue 1,
2003,
Page 30-37
Richard,
Sterling Melissa,
Contos Arun,
Sanyal Velimir,
Luketic R.,
Stravitz Mary,
Wilson A.,
Mills Mitchell,
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摘要:
The biochemical, virologic, and histologic spectrum of hepatitis C virus (HCV) in 66 consecutive patients with HIV-HCV coinfection and 119 HCV controls was compared: 86% of coinfected patients had CD4 counts >200 cells/mm3, 51% had a normal alanine aminotransferase (ALT) value, the mean HCV RNA titer was 5.7logIU/mL, 92% of coinfected patients were of genotype 1, and the mean histologic activity index was 6.86 with advanced fibrosis in 32% of patients. The biochemical, virologic, and histologic findings of HCV in coinfected patients were similar to those observed in HCV controls. For both groups of patients, no clinical, biochemical, or virologic factors could reliably identify patients with advanced fibrosis or cirrhosis, underscoring the importance of liver biopsy in the evaluation of these patients. The spectrum of liver disease in coinfection includes a significant proportion of patients with normal ALT values, and excluding these patients from previous studies has led to an overestimation of HCV disease severity.
ISSN:1525-4135
出版商:OVID
年代:2003
数据来源: OVID
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6. |
Health-Related Quality of Life After 1 Year of Highly Active Antiretroviral Therapy |
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JAIDS Journal of Acquired Immune Deficiency Syndromes,
Volume 32,
Issue 1,
2003,
Page 38-47
Patrizia,
Carrieri Bruno,
Spire Ségolène,
Duran Christine,
Katlama Dominique,
Peyramond Cécile,
François Geneviève,
Chêne Jean-Marie,
Lang Jean-Paul,
Moatti Catherine,
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摘要:
ObjectiveWe investigated the impact of the first year of highly active antiretroviral therapy (HAART) on health-related quality of life (HRQL).MethodsMedical data for patients in the French APROCO cohort were collected at enrollment (M0) and month 12 (M12). A self-administered questionnaire gathered information about HRQL (Medical Outcome Study 36-Item Short Form Health Survey) and toxicity-related symptoms. Using the twenty-fifth percentile of HRQL scales in the French population as a threshold, patients with normal values in at least three mental and three physical scales were considered to have a “normal HRQL.”ResultsOf the 1053 patients followed through M12, HRQL data at M0 and M12 were available for 654. Among the 233 patients with a normal baseline HRQL, 63 (27.0%) experienced a deterioration of HRQL at M12. Among the 421 patients with a low baseline HRQL, 121 achieved a normal HRQL at M12. Logistic regression showed that factors independently associated with a normal HRQL at M12 were normal baseline HRQL, baseline CD4 count <500 cells/mm3, time since HIV diagnosis <8 years, undetectable HIV-RNA at M12, and lower number of self-reported symptoms at M12.ConclusionAn assessment of HRQL should be integrated to efficacy outcomes to evaluate and compare long-term strategies properly and to optimize the durability of response to antiretroviral therapy.
ISSN:1525-4135
出版商:OVID
年代:2003
数据来源: OVID
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7. |
Incidence of and Risk Factors for Lipoatrophy (Abnormal Fat Loss) in Ambulatory HIV-1-Infected Patients |
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JAIDS Journal of Acquired Immune Deficiency Syndromes,
Volume 32,
Issue 1,
2003,
Page 48-56
Kenneth,
Lichtenstein Kathleen,
Delaney Carl,
Armon Douglas,
Ward Anne,
Moorman Kathleen,
Wood Scott,
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摘要:
To identify clinical factors associated with the incidence of HIV-1–associated lipoatrophy, HIV-1–infected patients in the HIV Outpatient Study (HOPS) were prospectively evaluated for clinical signs of lipoatrophy at two visits about 21 months apart. Development of lipoatrophy was analyzed in stratified and multivariate analyses for its relationship to immunologic, virologic, clinical, and drug treatment information for each patient. Of 337 patients with no lipoatrophy at Survey 1, 44 (13.1%) developed moderate or severe lipoatrophy between the two surveys. In multivariate analyses, significant risk factors for incident lipoatrophy were white race (OR = 5.2; 95% CI: 1.9–17.1;p= .003), CD4 T-lymphocyte count at Survey 2 less than 100 cells/mm3(OR = 4.2; 95% CI: 1.3–13.1;p= .013), and body mass index (BMI) less than 24 kg/m2(OR = 2.4; 95% CI: 1.1–5.4;p= .024). Analyses that controlled for the severity of HIV illness demonstrated no significant association with use of or time on any antiretroviral agent or class of agents and the development of lipoatrophy. Some host factors and factors associated with previous or current severity of HIV infection, especially CD4 T-lymphocyte cell count, appeared to have the strongest association with incidence of lipoatrophy.
ISSN:1525-4135
出版商:OVID
年代:2003
数据来源: OVID
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8. |
Limited Evolution of HIV Antiretroviral Drug Resistance-Associated Mutations During the Performance of Drug Resistance Testing |
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JAIDS Journal of Acquired Immune Deficiency Syndromes,
Volume 32,
Issue 1,
2003,
Page 57-61
Chris,
Birch Tracey,
Middleton Gillian,
Hales David,
Cooper Matthew,
Law Suzanne,
Crowe Jennifer,
Hoy Sean,
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摘要:
We investigated the evolution of HIV reverse transcriptase (RT)– and protease-associated antiretroviral (ARV) drug resistance mutations during the time taken to perform genotypic drug resistance testing. Thirty treatment-experienced patients who were adherent to therapy and who underwent genotypic drug resistance testing provided blood samples at randomization and when reviewing the test results (baseline). Patients remained on their existing therapy between randomization and baseline. The predominant HIV strains in 10 patients (33%) either lost and/or gained primary RT inhibitor (RTI)– or protease inhibitor (PI)–associated resistance mutations during the testing period. Of the 9 patients with RT mutations, 2 lost, 5 gained, and 2 both lost and gained RTI resistance mutations. One patient gained a significant PI-associated resistance mutation on an existing PI-resistant background. The evolution that occurred in the RT may have altered the effectiveness of subsequent ARV therapy in some patients. Neither viral load at randomization, ARV drug class used at randomization, time between collection of blood samples, duration of current therapy, nor number of ARV drugs used influenced gain or loss of resistance mutations. There was a significant association between duration of previous ARV therapy and gain of RTI-associated resistance mutations (p= .02), however. In general, our results suggest that patients should continue current therapy until test results are available. A few patients would be expected to gain ARV drug-associated resistance mutations during this time, however.
ISSN:1525-4135
出版商:OVID
年代:2003
数据来源: OVID
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9. |
Increase in Deaths Caused by HIV Infection Due to Changes in Rules for Selecting Underlying Cause of Death |
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JAIDS Journal of Acquired Immune Deficiency Syndromes,
Volume 32,
Issue 1,
2003,
Page 62-69
Richard,
Selik Robert,
Anderson Matthew,
McKenna Harry,
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摘要:
With implementation of theInternational Classification of Diseases, 10th Revision(ICD-10), for U.S. vital statistics in 1999, the criteria for selecting HIV infection as the underlying cause of death were expanded. To estimate the effect of ICD-10 rules on the number of deaths attributed to HIV infection, we applied a simplified version of ICD-10 rules to data on causes of death from all U.S. death certificates for 1998 (previously classified by rules of the 9th revision of ICD [ICD-9]) and calculated the resulting increase in deaths for which HIV infection was selected as the underlying cause. Of the 17,186 deaths in 1998 with any mention of HIV infection on the death certificate, ICD-10 rules selected HIV infection as the underlying cause for 15,145, which was 1,719 (13%) more than the 13,426 for which it had been selected by ICD-9 rules. The proportional increase differed by demographic group, being less among non-Hispanic blacks (9%) and Hispanics (13%) than among non-Hispanic whites (18%). Thus, comparison of deaths attributed to HIV infection in 1999 or later with those in 1998 or earlier should take into account the changes in ICD rules for selecting the underlying cause of death.
ISSN:1525-4135
出版商:OVID
年代:2003
数据来源: OVID
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10. |
Effect ofCCR5-&Dgr;32Heterozygosity on the Risk of Perinatal HIV-1 Infection: A Meta-Analysis |
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JAIDS Journal of Acquired Immune Deficiency Syndromes,
Volume 32,
Issue 1,
2003,
Page 70-76
Despina,
Contopoulos-Ioannidis Thomas,
O'Brien James,
Goedert Phillip,
Rosenberg John,
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摘要:
Several studies have investigated whether heterozygosity for a 32-basepair deletion in the CC chemokine receptor 5 gene (CCR5-&Dgr;32) affects susceptibility to perinatal HIV-1 infection, but results have been inconclusive. We performed a meta-analysis of published data from 11 studies of HIV-1 perinatally exposed children who were genotyped for theCCR5-&Dgr;32polymorphism. The crude overall HIV-1 infection rates, by simple data pooling, were 20% (one of five) amongCCR5-&Dgr;32homozygote children, 39% (131 of 335) amongCCR5-&Dgr;32heterozygote children, and 40% (1408 of 3526) among wild-typeCCR5homozygote children. Compared with wild-typeCCR5homozygotes, the random effects risk ratio forCCR5-&Dgr;32heterozygotes was 1.04 (95% confidence interval [CI], 0.92–1.17) among all children (N= 3861) and 1.03 (95% CI, 0.90–1.17) among those of European descent (n= 2890). Results were similar when adjusted for the available data on theCCR2–64Ipolymorphism (n= 1542). The meta-analysis clarifies that perinatal infection is not significantly altered by heterozygosity forCCR5-&Dgr;32in the child.
ISSN:1525-4135
出版商:OVID
年代:2003
数据来源: OVID
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