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Pneumonitis in bone marrow transplant recipients results from a local immune response
Author(s) -
MILBURN H. J.,
BOIS R. M. DU,
PRENTICE H. G.,
POULTER L. W.
Publication year - 1990
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1111/j.1365-2249.1990.tb03323.x
Subject(s) - immunology , cytotoxic t cell , cd8 , immune system , cd5 , bone marrow , il 2 receptor , biology , bronchoalveolar lavage , antigen , cd38 , lymphocyte , t lymphocyte , t cell , medicine , lung , stem cell , microbiology and biotechnology , in vitro , biochemistry , cd34
SUMMARY Eighteen recipients of allogeneic T cell‐depleted bone marrow who developed 22 episodes of interstitial pneumonitis were investigated by bronchoalveolar lavage for the cause of pneumonitis. The cells obtained were examined using a panel of monoclonal antibodies with immunocytochemical techniques to identify lymphocyte subsets and the presence of surface molecules indicative of lymphocyte activation. The majority of patients had an excess of lymphocytes in lavage and most of these cells were positively stained with the McAb recognizing the CD8 antigen (suppressor/cytotoxic type T cells). Although the proportions of CD4 + (helper type) T cells were below normal, the absolute numbers were within normal limits, thus the CD4:CD8 ratio was consistently 1:1 or less. A large proportion of the CD8 + cells displayed HLA‐DR molecules (RFDR1 + ), interleukin‐2 (IL‐2) receptors (CD25 + ) and high concentration of CD7 antigen (RFT2 + ). Further analysis revealed that most CD8 + cells were CD5 + (RFT1 + ) yet a large proportion (20–40%) were CD5 − . A majority of CD8 + cells was also CD38 + (RFT10 + ) and Leu7 + . No clear correlation between the emergence of a raised proportion of activated CD8 + cells and diagnosed cytomegalovirus infection was found. These results demonstrate, however, that cells with the phenotype of the resident T cells of the bronchial epithelium (CD8 + CD5 − ) emerge to the air spaces and express activation markers. This raises the intriguing paradox of an aggressive local immune response occurring in an otherwise immunosuppressed group of patients.

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