Document 0280 DOCN M94A0280 TI Clinical and immunologic evaluation of HIV-infected patients treated with dinitrochlorobenzene. DT 9412 AU Stricker RB; Elswood BF; Goldberg B; Dumlao C; Van Elk J; Henry J; Winger EE; Epstein WL; HemaCare Corporation, San Francisco, CA 94108. SO J Am Acad Dermatol. 1994 Sep;31(3 Pt 1):462-6. Unique Identifier : AIDSLINE MED/94358210 AB BACKGROUND: Promotion of cell-mediated immunity appears to be an important goal in the control of HIV infection. Topical dinitrochlorobenzene (DNCB) stimulates systemic cell-mediated immunity via the induction of cutaneous delayed-type hypersensitivity. OBJECTIVE: Our goal was to evaluate the clinical and immunologic effects of chronic DNCB application in a group of 24 HIV-infected patients. METHODS: We observed the patients for a mean of 28 months (range, 14 to 44 months). Of the 24 patients, 13 continued weekly DNCB application throughout the study (the compliant group), and 11 discontinued DNCB use after a mean of 10.9 months (the noncompliant group). RESULTS: Two of the 13 compliant patients progressed to AIDS; none of these patients died. In contrast, AIDS developed in 5 of the 11 noncompliant patients and four of these patients died. Analysis of lymphocyte subsets revealed significant increases in natural killer cells and activated/cytotoxic CD8 T-cell subsets in the compliant group. In contrast, these cellular immune-related lymphocyte subsets decreased in the noncompliant subjects. Although CD4 T-cell levels decreased in both groups, there was a significantly greater drop in the noncompliant patients. CD8+CD38+ T cells increased significantly in both groups. CONCLUSION: Chronic DNCB application appears to have a beneficial clinical and immunomodulatory effect in HIV-infected patients. DE Acquired Immunodeficiency Syndrome/IMMUNOLOGY Antigens, CD/ANALYSIS CD4-CD8 Ratio Dinitrochlorobenzene/*THERAPEUTIC USE Flow Cytometry Human HIV Infections/DRUG THERAPY/*IMMUNOLOGY Immunity, Cellular Lymphocyte Subsets Male Patient Compliance Support, Non-U.S. Gov't JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).