Volume 37, Issue 4 pp. 474-478
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Interleukin-2 receptor positive T and B cells in children with acute severe asthmatic attack

MAKOTO NABETANI

Corresponding Author

MAKOTO NABETANI

Department of Pediatrics, Kure Mutual Aid Hospital, Kure, Japan

Department of Physiology, School of Medicine, Kobe University, 7-5 Kusunoki-cho, Chuouku, Kobe 650, Japan.Search for more papers by this author
TAKEMI YAMASAKI

TAKEMI YAMASAKI

Department of Pediatrics, Kure Mutual Aid Hospital, Kure, Japan

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AIJU KAMEDA

AIJU KAMEDA

Department of Pediatrics, Kure Mutual Aid Hospital, Kure, Japan

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OSAMU OKAMOTO

OSAMU OKAMOTO

Department of Pediatrics, Kure Mutual Aid Hospital, Kure, Japan

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TAKUMI KISHIMOTO

TAKUMI KISHIMOTO

Department of Allergology, Kure Mutual Aid Hospital, Kure, Japan

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First published: August 1995
Citations: 1

Abstract

Subpopulations of interleukin-2 receptor (IL-2R)-positive CD4 and CD8 T cells and IL-2R+ CD20 B cells in the peripheral blood lymphocytes as well as serum concentrations of soluble IL-2R (sIL2R) were measured in children aged 1–7 years who suffered acute severe asthmatic attack. Subpopulations of CD4+ IL-2R+ cells, CD8+ IL-2R+ cells and CD20+ IL-2R+ cells in the peripheral blood lymphocytes at acute severe asthmatic attack phase were significantly higher than those at non-asthmatic attack phase (P < 0.02, P < 0.03 and P < 0.02, respectively).

Subpopulations of CD20+ IL-2R+ cells in the peripheral blood lymphocytes significantly decreased 5–10 days after acute severe asthmatic attack (at recovery phase, P < 0.02) and were significantly correlated with clinical severity of asthmatic attack (P < 0.05).

These results indicated that activation of both T cells and B cells was important in the pathogenesis of acute asthmatic attack in young children.

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