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Article has an altmetric score of 12

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Referenced in 3 patents
Referenced in 2 clinical guideline sources
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Research Article Free access | 10.1172/JCI116633

Influence of grass pollen immunotherapy on cellular infiltration and cytokine mRNA expression during allergen-induced late-phase cutaneous responses.

V A Varney, Q A Hamid, M Gaga, S Ying, M Jacobson, A J Frew, A B Kay, and S R Durham

Department of Allergy and Clinical Immunology, National Heart & Lung Institute, London, United Kingdom.

Find articles by Varney, V. in: PubMed | Google Scholar

Department of Allergy and Clinical Immunology, National Heart & Lung Institute, London, United Kingdom.

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Department of Allergy and Clinical Immunology, National Heart & Lung Institute, London, United Kingdom.

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Department of Allergy and Clinical Immunology, National Heart & Lung Institute, London, United Kingdom.

Find articles by Ying, S. in: PubMed | Google Scholar

Department of Allergy and Clinical Immunology, National Heart & Lung Institute, London, United Kingdom.

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

Department of Allergy and Clinical Immunology, National Heart & Lung Institute, London, United Kingdom.

Find articles by Frew, A. in: PubMed | Google Scholar

Department of Allergy and Clinical Immunology, National Heart & Lung Institute, London, United Kingdom.

Find articles by Kay, A. in: PubMed | Google Scholar

Department of Allergy and Clinical Immunology, National Heart & Lung Institute, London, United Kingdom.

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Published August 1, 1993 - More info

Published in Volume 92, Issue 2 on August 1, 1993
J Clin Invest. 1993;92(2):644–651. https://doi.org/10.1172/JCI116633.
© 1993 The American Society for Clinical Investigation
Published August 1, 1993 - Version history
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Abstract

We have studied the influence of grass pollen immunotherapy on cellular infiltration and cytokine mRNA expression during allergen-induced late-phase cutaneous responses. In a double-blind, placebo-controlled trial of immunotherapy in 40 adult hay fever sufferers, clinical improvement was accompanied by a decrease in the size of the late-phase skin response. When the immunotherapy-treated group was compared with the placebo group, analysis of skin biopsies obtained 24 h after intradermal allergen revealed a significant reduction in the number of infiltrating CD3+ (P = 0.04) and CD4+ (P = 0.009) cells and a trend for a decrease in EG2+ eosinophils (P = 0.08). Treatment did not influence allergen-induced recruitment of CD8+ cells, neutrophils, or macrophages. Unexpected increases in expression of CD25 (P = 0.006) and HLA-DR (P = 0.007) were observed in the actively treated group. In situ hybridization using a panel of riboprobes demonstrated "TH2-type" (IL-4, IL-5) cytokine mRNA responses in both groups of patients. In contrast, significant hybridization for IL-2 (8/16 patients, P = 0.02) and for interferon-gamma (6/16 patients, P = 0.04) was observed only in the actively treated group. These findings indicate that immunotherapy is associated with suppression of allergen-induced CD4+ T lymphocyte infiltration, but among the cells that are recruited, there is upregulation of CD25 and HLA-DR. At least in this model, immunotherapy does not appear to affect expression of TH2-pattern cytokines in response to allergen exposure, but expression of mRNA for Th1-type cytokines was enhanced in half of the patients. The results support the view that immunotherapy may possibly be working through induction of T cell tolerance.

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Referenced in 3 patents
Referenced in 2 clinical guideline sources
45 readers on Mendeley
See more details