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Research Article Free access | 10.1172/JCI115428

Requirement of CD4-positive T cells for cellular recruitment to the lungs of mice in response to a particulate intratracheal antigen.

J L Curtis, P K Byrd, M L Warnock, and H B Kaltreider

Respiratory Care Section, San Francisco Veterans Administration Medical Center, California.

Find articles by Curtis, J. in: PubMed | Google Scholar

Respiratory Care Section, San Francisco Veterans Administration Medical Center, California.

Find articles by Byrd, P. in: PubMed | Google Scholar

Respiratory Care Section, San Francisco Veterans Administration Medical Center, California.

Find articles by Warnock, M. in: PubMed | Google Scholar

Respiratory Care Section, San Francisco Veterans Administration Medical Center, California.

Find articles by Kaltreider, H. in: PubMed | Google Scholar

Published October 1, 1991 - More info

Published in Volume 88, Issue 4 on October 1, 1991
J Clin Invest. 1991;88(4):1244–1254. https://doi.org/10.1172/JCI115428.
© 1991 The American Society for Clinical Investigation
Published October 1, 1991 - Version history
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Abstract

To determine whether CD4+ T cells participate in the recruitment of other lymphocyte subsets to the lungs, we examined pulmonary immune responses in C57BL/6 mice treated in vivo with the MAb GK1.5, either intact (which depletes CD4+ cells) or as F(ab')2 fragments (which block CD4 molecules). After intratracheal challenge with sheep erythrocytes, antigen-primed mice treated with intact GK1.5 had marked decreases in lymphocytes and macrophages in bronchoalveolar lavage fluid and minimal parenchymal inflammation, compared to primed mice treated with an isotype-matched irrelevant antibody or with no antibody. At 7 d after challenge, flow cytometric analysis showed that numbers of Thy 1.2+ and B220+ cells, but not of CD8+ cells, were markedly decreased in lavage fluid of CD4-depleted mice. Similar suppression of the pulmonary immune response to intratracheal challenge was found in primed mice injected repeatedly with F(ab')2 fragments of GK1.5, which did not deplete CD4+ T cells, and in athymic mice. These findings indicate that, in response to a single intratracheal antigen challenge, recruitment to the lungs of leukocytes other than CD8+ T cells depends largely on CD4+ T cells, possibly because of signals requiring T cell activation via interactions with antigen-presenting cells.

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