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. 1984;17(2):112-6.
doi: 10.1007/BF00200046.

Imbalances of T-cell subsets in monoclonal gammopathies

Imbalances of T-cell subsets in monoclonal gammopathies

L Bergmann et al. Cancer Immunol Immunother. 1984.

Abstract

In 42 patients with untreated or treated multiple myeloma (MM) or benign monoclonal gammopathy (BMG) the lymphocytes and T lymphocyte subsets were determined by monoclonal antibodies and other surface markers. In untreated MM, the T cells (1077/microliters vs 1439/microliters, P less than 0.01) and especially the OKT4+ lymphocytes (700/microliters vs 950/microliters, P less than 0.05) were significantly reduced compared with a control group. The OKT8+ cells were slightly but not significantly decreased. In previously treated MM, the loss of T cells was more pronounced than in the untreated group and was primarily caused by a further reduction of OKT4+ cells. Patients with BMG revealed decreased OKT8+ lymphocytes (304/microliters vs 502/microliters, P less than 0.001), whereas the OKT4+ cells were within the normal range. Therefore, the OKT4/OKT8 ratio was significantly elevated compared with that in untreated MM patients and normal controls (3.31 vs 2.06 vs 2.13; P less than 0.005). To sum up, in MM the results revealed a reduction of T cells, mainly of OKT4+ cells, which is intensified by chemotherapy and persists even after a long therapy-free interval. The different findings of T cell subsets in BMG and MM may be a helpful criterion to differentiate between BMG and MM.

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References

    1. Abu T, Balch CM. A differentiation antigen of human NK and K cells identified by a monoclonal antibody (HNK-1) J Immunol. 1981;127:1024. - PubMed
    1. Aiuiti F, Cerottini JC, Coombs RRA, Cooper M, Dickler HB, Froland SS, Fudenberg HH, Greaves MF, Grey HM, Kunkel HG, Natvig JB, Preud'homme JL, Rabellino E, Ritts RE, Rowe DS, Seligman M, Siegal FP, Sterns-Wärd J, Terry WD, Wybran J. Identification, enumeration and isolation of B and T lymphocytes from human peripheral blood. Scand J Immunol. 1974;3:173. doi: 10.1111/j.1365-3083.1974.tb01245.x. - DOI - PubMed
    1. Bergmann L, Mitrou PS, Cherdron T, Holloway K, Jost J, Timm V, Zerth G. Expression of Ia-like antigen in lymphatic leukaemias and non-Hodgkin lymphomas in correlation with other surface markers. Scand J Haematol. 1982;29:224. doi: 10.1111/j.1600-0609.1982.tb00587.x. - DOI - PubMed
    1. Broder S, Humphrey R, Durm M, Blackman M, Meade B, Goldman C, Strober W, Waldmann T. Impaired synthesis of polyclonal (non-paraprotein) immunoglobulins by circulating lymphocytes from patients with multiple myeloma. N Engl J Med. 1975;293:887. doi: 10.1056/NEJM197510302931801. - DOI - PubMed
    1. Cone L, Uhr JW. Immunological deficiency disorders associated with chronic lymphocytic leukemia and multiple myeloma. J Clin Invest. 1964;43:2241. doi: 10.1172/JCI105098. - DOI - PMC - PubMed

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