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Research Article Free access | 10.1172/JCI107257

B and T Lymphocytes in Primary Immunodeficiency Disease in Man

Kazimiera J. Gajl-Peczalska, Byung H. Park, W. Douglas Biggar, and Robert A. Good

Department of Pathology, University of Minnesota, Minneapolis, Minnesota 55455

Department of Pediatrics, University of Minnesota, Minneapolis, Minnesota 55455

Find articles by Gajl-Peczalska, K. in: PubMed | Google Scholar

Department of Pathology, University of Minnesota, Minneapolis, Minnesota 55455

Department of Pediatrics, University of Minnesota, Minneapolis, Minnesota 55455

Find articles by Park, B. in: PubMed | Google Scholar

Department of Pathology, University of Minnesota, Minneapolis, Minnesota 55455

Department of Pediatrics, University of Minnesota, Minneapolis, Minnesota 55455

Find articles by Biggar, W. in: PubMed | Google Scholar

Department of Pathology, University of Minnesota, Minneapolis, Minnesota 55455

Department of Pediatrics, University of Minnesota, Minneapolis, Minnesota 55455

Find articles by Good, R. in: PubMed | Google Scholar

Published April 1, 1973 - More info

Published in Volume 52, Issue 4 on April 1, 1973
J Clin Invest. 1973;52(4):919–928. https://doi.org/10.1172/JCI107257.
© 1973 The American Society for Clinical Investigation
Published April 1, 1973 - Version history
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Abstract

B- and T-cell populations in 32 patients with different forms of primary immunodeficiency disease were studied. The B-cells in peripheral blood were investigated with respect to surface immunoglobulins by means of immunofluorescence. The T-cell function was studied utilizing quantitation of proliferative response to phytochemagglutinin (PHA)1 and delayed allergy to various antigens. In 10 patients lymph node lymphocytes were also evaluated 11 male children with infantile x-linked agammaglobulinemia were divided into two subgroups. One did not show immunoglobulin spots on peripheral blood lymphocytes at all, the other contained a very low percentage of IgM- and occasionally IgA bearing lymphocytes. Eight patients with common variable immunodeficiency had moderately decreased percentages of peripheral blood and lymph node lymphocytes with surface immunoglobulins, but these patients lacked immunoglobulin secreting cells. Four cases of isolated IgA deficiency had normal or high percentages, and two cases of ataxia-telangiectasia had high percentages of lymphocytes with IgA in so called receptor distribution in both peripheral blood and lymph nodes. In three patients with infantile combined immunodeficiency that had been corrected by marrow transplantation, the percentages of Ig-bearing lymphocytes increased to normal or high levels together with establishment of functional T-cell population and ultimate secretion of serum immunoglobulins. One case of Di George syndrome reconstituted by fetal thymus transplant showed gradual decrease of B lymphocytes in circulation parallel to restoration of T-cell population.

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