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Polyclonal activation of immunoglobulin secretion without prior DNA synthesis in human B lymphocytes induced by Klebsiella pneumoniae

W. L. Gross*, A. Rucks, G. Hahn, U. Ullmann

*Korrespondierende/r Autor/-in für diese Arbeit

Abstract

The capacity of various cell preparations of Klebsiella pneumoniae K43 (Klebs) to induce [3H]thymidine uptake and immunoglobulin (Ig) secretion by human mononuclear blood cells (MNC) and their lymphocyte subpopulations was investigated. All Klebs preparations were virtually devoid of mitogenic properties, in contrast to control preparations of pokeweed mitogen (PWM) and group A streptococcal cell membranes (A-ScM). Klebs induced differentiation of B cells into Ig-secreting cells. B-cell populations that were sufficiently depleted of T cells to be unresponsive to A-ScM ("highly purified B cells") showed a marked response to Klebs. Similarly, the number of plaque-forming cells (PFC) in Klebs-driven cultures did not change after restitution of T cells, whereas the presence of restituted T cells augmented the B-cell response to PWM and A-ScM. Radical removal of adherent MNC ("monocytes"), however, completely abrogated the PFC response and [3H]thymidine uptake of both MNC activated by Klebs and MNC activated by PWM or A-ScM.

OriginalspracheEnglisch
ZeitschriftClinical Immunology and Immunopathology
Jahrgang27
Ausgabenummer2
Seiten (von - bis)261-271
Seitenumfang11
ISSN0090-1229
DOIs
PublikationsstatusVeröffentlicht - 05.1983

Fördermittel

The expert technical assistance of Mrs. Rautmann and Mr. Utecht is gratefully acknowledged. Supported by Grant Gr609/3-3 from the Deutsche Forschungsgemeinschaft and a grant from the Verein zur Forderung der Erforschung und Bekampfung rheumatischer Erkrankungen.

UN SDGs

Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

  1. SDG 3 – Gesundheit und Wohlergehen
    SDG 3 – Gesundheit und Wohlergehen

Strategische Forschungsbereiche und Zentren

  • Forschungsschwerpunkt: Infektion und Entzündung - Zentrum für Infektions- und Entzündungsforschung Lübeck (ZIEL)

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