Document 0102 DOCN M95A0102 TI In vitro T cell function, delayed-type hypersensitivity skin testing, and CD4+ T cell subset phenotyping independently predict survival time in patients infected with human immunodeficiency virus. DT 9510 AU Dolan MJ; Clerici M; Blatt SP; Hendrix CW; Melcher GP; Boswell RN; Freeman TM; Ward W; Hensley R; Shearer GM; Department of Infectious Diseases, Wilford Hall Medical Center,; Lackland Air Force Base, TX 78236-5300, USA. SO J Infect Dis. 1995 Jul;172(1):79-87. Unique Identifier : AIDSLINE MED/95318562 AB Human immunodeficiency virus type 1 (HIV-1)-infected patients (n = 335) in the US Air Force HIV Natural History Program were followed for 3 years (mean) after skin testing, immunophenotyping of CD4+ cell subsets, and measurement of in vitro interleukin-2 production after stimulation by phytohemagglutinin, alloantigens, tetanus toxoid, and influenza A virus. The T cell functional assay predicted survival time (P < .001) and time for progression to AIDS (P = .014). Skin testing for tetanus, mumps, and Candida antigen and the total number of positive tests (P < .001 for each) stratified patients for survival time. In a multivariable proportional hazards model, the T cell functional assay (P = .008), the absolute number of CD4+ T cells (P = .001), the percentage of CD4+ CD29+ cells (P = .06), and the number of reactive skin tests (P < .001) predicted survival time. Thus, cellular immune functional tests have significant predictive value for survival time in HIV-1-infected patients independent of CD4+ cell count. DE Acquired Immunodeficiency Syndrome/IMMUNOLOGY/MORTALITY/ *PHYSIOPATHOLOGY Adult Comparative Study CD4 Lymphocyte Count CD4-Positive T-Lymphocytes/*IMMUNOLOGY Female Human *Hypersensitivity, Delayed HIV Infections/*IMMUNOLOGY/*MORTALITY Immunity, Cellular Male Middle Age Military Personnel Multivariate Analysis Predictive Value of Tests Prognosis Proportional Hazards Models Skin Tests Support, Non-U.S. Gov't Support, U.S. Gov't, Non-P.H.S. Support, U.S. Gov't, P.H.S. Survival Rate T-Lymphocytes/*IMMUNOLOGY Time Factors United States JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).