Document 1124 DOCN M94A1124 TI Lymphocyte function and cytokines in HIV+ patients treated on AZT or ddI. DT 9412 AU Raise E; Fondacaro A; Guerra L; Chen CH; Cicognani MA; Schiattone ML; Martuzzi M; Gritti FM; Infect. Dis. Dept., Maggiore Hospital, Bologna, Italy. SO Int Conf AIDS. 1994 Aug 7-12;10(2):203 (abstract no. PB0825). Unique Identifier : AIDSLINE ICA10/94371451 AB OBJECTIVE: To investigate lymphocyte function and serum cytokines in HIV+ patients (pts), treated on AZT or ddI. METHODS: We studied: 20 asymptomatic pts, at high risk of evolution (HR), defined as CD4 < 500/cmm and low anti-p24 Ab, elevated B2 M. and p24Ag, treated on AZT 250 mg b.i.d.; 22 ARC and 10 AIDS: 12 randomly, and 20, AZT-intolerant/resistant, treted on ddI 250-375 mg b.i.d.; 20 ARC and 10 AIDS on AZT 200 mg q.6-8 h/day. Lymphocytes, CD4, CD8, CD16 CD56 absolute number; NK-activity (NKA); lymphocyte prolipheration by PHA (PHA-LP), were evaluated at baseline (Bl) and at 3rd and 6th momth (m); serum IL-2. TNF-alpha, IL-6, p24Ag and soluble lymphocyte receptors, IL-2sR, CD8sR, at Bl and 3rd m. RESULTS: In HR and ARC pts, Bl NKA and PHA-LP were > 50% reduced; IL-2 was significantly (S) (T student test) elevated, in HR > than ARC, where TNF-a was S increased. In AIDS, NKA and PHA-LP were more depressed, IL-2 was low; TNF-alpha and IL-6 were S elevated, at Bl. ZDV and ddI reduced p24 Ag load in all, increased S CD4, NKA and PHA-LP, only in ARC pts, with increase of IL-2, found also in HR, not in AIDS, where only p24 Ag and IL-6 decreased. IL-2sR and CD8sR were increased at Bl in all, and did reduce after ZDV and in AIDS. DISCUSSION AND CONCLUSIONS: Cytokine variability, in the infection, might condition Th1 or Th2 prevalence, and lymphocyte function. During latency, NKA and PHA-LP are compromised, while IL-2 is elevated, protecting from opportunistic infections even in ARC. Probably CTL are used instead of NK. AZT/ddI restore NKA and PHA-LP function in ARC pts and, reducing viral load, support lymphocyte function. They also reduce the immune activation expressed by the increase of circulating IL-2sR and CD8rS. DE Acquired Immunodeficiency Syndrome/DRUG THERAPY/IMMUNOLOGY AIDS-Related Complex/DRUG THERAPY/IMMUNOLOGY Cytokines/*BLOOD Didanosine/*THERAPEUTIC USE Human HIV Core Protein p24/ANALYSIS HIV Seropositivity/*DRUG THERAPY/IMMUNOLOGY Interleukins/BLOOD Killer Cells, Natural/IMMUNOLOGY Lymphocyte Transformation Lymphocytes/*IMMUNOLOGY T-Lymphocyte Subsets Tumor Necrosis Factor/ANALYSIS Zidovudine/*THERAPEUTIC USE CLINICAL TRIAL MEETING ABSTRACT RANDOMIZED CONTROLLED TRIAL SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).