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Research Article Free access | 10.1172/JCI107342

Phagocytic Function of Polymorphonuclear Leukocytes in Rheumatic Diseases

Robert A. Turner, H. Ralph Schumacher, and Allen R. Myers

Arthritis Section of the Department of Medicine, Gray School of Medicine of Wake Forest University, Winston-Salem, North Carolina 27103

Arthritis Section of the Department of Medicine, The University of Pennsylvania School of Medicine, and Philadelphia Veterans Administration Hospital, Philadelphia, Pennsylvania 19104

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

Arthritis Section of the Department of Medicine, Gray School of Medicine of Wake Forest University, Winston-Salem, North Carolina 27103

Arthritis Section of the Department of Medicine, The University of Pennsylvania School of Medicine, and Philadelphia Veterans Administration Hospital, Philadelphia, Pennsylvania 19104

Find articles by Schumacher, H. in: PubMed | Google Scholar

Arthritis Section of the Department of Medicine, Gray School of Medicine of Wake Forest University, Winston-Salem, North Carolina 27103

Arthritis Section of the Department of Medicine, The University of Pennsylvania School of Medicine, and Philadelphia Veterans Administration Hospital, Philadelphia, Pennsylvania 19104

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

Published July 1, 1973 - More info

Published in Volume 52, Issue 7 on July 1, 1973
J Clin Invest. 1973;52(7):1632–1635. https://doi.org/10.1172/JCI107342.
© 1973 The American Society for Clinical Investigation
Published July 1, 1973 - Version history
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Abstract

Phagocytosis of yeast particles by peripheral blood and synovial fluid neutrophils was compared in the sera and synovial fluids from 16 osteoarthritis, 23 rheumatoid arthritis, and 12 miscellaneous arthritis patients. Phagocytosis by normal peripheral blood neutrophils was decreased equally and significantly in all synovial fluids. All synovial fluid neutrophils demonstrated decreased phagocytic capacity in all media. Rheumatoid arthritis synovial fluid neutrophils showed significantly less phagocytosis than miscellaneous arthritis synovial fluid neutrophils. Normal peripheral blood neutrophils which in vitro had previously ingested monosodium urate crystals or oil red O, subsequently exhibited a normal yeast phagocytic capacity. Normal peripheral blood neutrophils, which had ingested preformed immunoglobulin G-rheumatoid factor complexes exhibited significantly less yeast phagocytic capacity than control cells or cells preincubated with the individual complex components. There was a significant correlation between the log of the reciprocal of the rheumatoid factor titer in sera used to produce complexes and the phagocytic capacity exhibited by test neutrophils. Ingestion of immunoglobulin G-rheumatoid factor complexes may be important in the production of the cellular phagocytic defect which this study has demonstrated in rheumatoid arthritis synovial fluid neutrophils.

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