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LYSIS OF ERYTHROCYTES BY COMPLEMENT IN THE ABSENCE OF ANTIBODY

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Götze, Otto, Müller-Eberhard, Hans J.·1970·The Journal of Experimental Medicine

Abstract

A new pathway of complement-mediated hemolysis has been described. It is independent of antibody and does not require binding of the first four complement components to the target-cell surface. The actual attack of the target cell begins with the attachment of C5, C6, and C7. The binding reaction is catalyzed by C4, 2, 3, an enzyme which may be formed in cell-free solution. C4, 2, 3 may effect binding of C5, 6, 7 by acting from the fluid phase or from the surface of another cell to which it is specifically bound (EAC 4, 2, 3). In either case, the resulting product is EC5, 6, 7 which is susceptible to lysis by C8 and C9. Erythrocytes from patients with paroxysmal nocturnal hemoglobinuria (PNH) were particularly susceptible to lysis by the above described mechanism. PNH cells, but not normal human erythrocytes, could also be lysed through activation of complement by cobra factor. These observations allow the operational distinction of an activation and an attack mechanism of complement.

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Metadata

Authors
Götze, O., & Müller-Eberhard, H. J.
Venue
The Journal of Experimental Medicine
Published
1970-11-01
Volume
132
Issue
5
Pages
898-915
ISSN
  • 0022-1007 (ISSN-L)
  • 1540-9538
OpenAlex
W1980755391
Cited by
180
References
0
FWCI
6.06
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: LYSIS OF ERYTHROCYTES BY COMPLEMENT IN THE ABSENCE OF ANTIBODY. https://app.cochat.ai/papers/10.1084/jem.132.5.898
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Götze, O., & Müller-Eberhard, H. J. (1970). LYSIS OF ERYTHROCYTES BY COMPLEMENT IN THE ABSENCE OF ANTIBODY. The Journal of Experimental Medicine. https://doi.org/10.1084/jem.132.5.898

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.