DECREASED DTH RESPONSE TO RECALL ANTIGENS IN MICE INJECTED WITH HUMAN-IMMUNODEFICIENCY-VIRUS TYPE 1-INFECTED U937 CELLS AND INFECTED WITH CANDIDA-ALBICANS

Citation
R. Lande et al., DECREASED DTH RESPONSE TO RECALL ANTIGENS IN MICE INJECTED WITH HUMAN-IMMUNODEFICIENCY-VIRUS TYPE 1-INFECTED U937 CELLS AND INFECTED WITH CANDIDA-ALBICANS, Journal of biological regulators and homeostatic agents, 12(1-2), 1998, pp. 33-37
Citations number
33
Categorie Soggetti
Endocrynology & Metabolism",Physiology,Immunology,"Medicine, Research & Experimental",Biology
ISSN journal
0393974X
Volume
12
Issue
1-2
Year of publication
1998
Pages
33 - 37
Database
ISI
SICI code
0393-974X(1998)12:1-2<33:DDRTRA>2.0.ZU;2-7
Abstract
In previous studies, we have reported that the intraperitoneal (i.p.) injection of HIV-1 infected human U937 cells into normal mice resulted in long-term persistence of anti-HIV antibodies and in a small percen tage (10-20%) of HIV-1 infected animals at 6-12 months after the injec tion. The study reported here was undertaken to detect T immune defect s in U937-HIV-1-injected mice. Eight months after the initial injectio n, a marked decrease in DTH response against U937 cells was detected i n HIV injected animals. In addition, a consistent decrease in DTH resp onse against a soluble mannoprotein antigen of Candida albicans cell w all (MP-F2) was also observed in U937-HIV-1-injected mice, chronically infected with a low-virulent strain of the fungus. No decrease in DTH response was observed in control-injected animals. These data indicat e that U937-HIV-1-injected mice become unable to mount a normal antige n-specific immune response. Although the mechanisms involved in the ge neration of these T cell defects remain unclear, these events appear t o be somehow related to the HIV-I infection and should be considered i n the current studies of HIV-1 infection with transgenic mice.