Selective CD8+ T cells accumulate in the lungs of patients with allergic asthma after allergen bronchoprovocation

WahlstrÖM, DahlÉN, Ihre, Wigzell… - Clinical & …, 1998 - Wiley Online Library
WahlstrÖM, DahlÉN, Ihre, Wigzell, Grunewald, Eklund
Clinical & Experimental Immunology, 1998Wiley Online Library
Our objective was to study whether CD4+ or CD8+ T cells expressing particular T cell
receptors (TCR) would accumulate in the lungs of patients with allergic asthma following
allergen exposure. We thus analysed the TCR Vα and Vβ gene usage of CD4+ and CD8+
lung and peripheral blood lymphocytes (PBL) of eight patients with allergic asthma before
and 4 days after inhalation challenge with the relevant allergen. Lung cells obtained by
bronchoalveolar lavage (BAL) and paired PBL samples were analysed by flow cytometry …
Our objective was to study whether CD4+ or CD8+ T cells expressing particular T cell receptors (TCR) would accumulate in the lungs of patients with allergic asthma following allergen exposure. We thus analysed the TCR Vα and Vβ gene usage of CD4+ and CD8+lung and peripheral blood lymphocytes (PBL) of eight patients with allergic asthma before and 4 days after inhalation challenge with the relevant allergen. Lung cells obtained by bronchoalveolar lavage (BAL) and paired PBL samples were analysed by flow cytometry using a panel of anti‐TCR V‐specific monoclonal antibodies that encompass ≈ 50% of the T cell repertoire. Lung‐limited T cell expansions were recorded in both the CD4+and the CD8+subsets. In BAL CD8+, out of a total of 126 analyses, the number of T cell expansions increased from two to 11 after challenge, some of them dramatic. In BAL CD4+the frequency of expansions was moderately increased already before challenge, but remained unchanged. A few expansions that tended to persist were noted in PBL CD8+. When analysing the overall change in TCR V gene usage the largest changes were also recorded in the BAL CD8+subset. Specific interactions between T cells and antigens may lead to an increased frequency of T cells using selected TCR V gene segments. In this study we demonstrate that following allergen bronchoprovocation in allergic asthmatic subjects, T cell expansions preferentially emerge in the lung CD8+T cell subset.
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