TY - JOUR
T1 - Helper T-cell responses in children infected with human immunodeficiency virus type 1
AU - Roilides, Emmanuel
AU - Clerici, Mario
AU - DePalma, Louis
AU - Rubin, Marc
AU - Pizzo, Philip A.
AU - Shearer, Gene M.
PY - 1991
Y1 - 1991
N2 - Helper T-cell function was evaluated in 34 children infected with human immunodeficlency virus type 1, by assessing interleukin-2 production after stimulation of peripheral blood mononuclear cells with recall antigens (influenza virus, tetanus toxoid), allogeneic HLA, and phytohemagglutinin. In addition, helper T-cell function was correlated retrospectively with the incidence of opportunistic and bacterial infections. Four patterns of helper T-cell function were observed: (1) 7 (21%) of the 34 children responded to all stimuli, (2) 7 (21%) of them responded to alloantigens and phytohemagglutinin but not to recall antigens, (3) 7 (21%) responded to phytohemagglutinin but not to recall antigens or alloantigens, and (4) 13 (37%) did not respond to any of these stimuli. There were no significant differences related to different routes of acquisition among patients. Patients with functional helper T-cell defects had a history of more opportunistic (p=0.03) and bacterial (p
AB - Helper T-cell function was evaluated in 34 children infected with human immunodeficlency virus type 1, by assessing interleukin-2 production after stimulation of peripheral blood mononuclear cells with recall antigens (influenza virus, tetanus toxoid), allogeneic HLA, and phytohemagglutinin. In addition, helper T-cell function was correlated retrospectively with the incidence of opportunistic and bacterial infections. Four patterns of helper T-cell function were observed: (1) 7 (21%) of the 34 children responded to all stimuli, (2) 7 (21%) of them responded to alloantigens and phytohemagglutinin but not to recall antigens, (3) 7 (21%) responded to phytohemagglutinin but not to recall antigens or alloantigens, and (4) 13 (37%) did not respond to any of these stimuli. There were no significant differences related to different routes of acquisition among patients. Patients with functional helper T-cell defects had a history of more opportunistic (p=0.03) and bacterial (p
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U2 - 10.1016/S0022-3476(05)80033-2
DO - 10.1016/S0022-3476(05)80033-2
M3 - Article
C2 - 1673468
AN - SCOPUS:0025810157
VL - 118
SP - 724
EP - 730
JO - Journal of Pediatrics
JF - Journal of Pediatrics
SN - 0022-3476
IS - 5
ER -