|
|
||||||||
Department of Experimental Chemotherapy, Institut Pasteur, Paris, France
Abstract
The bactericidal effect of normal mouse serum, generally ascribed to natural "O" antibodies, can be removed by absorption with rough microorganisms. Passive hemagglutination tests disclose the presence of thermolabile, non-agglutinating "R" antibodies in normal mouse serum; titers in germ-free animals are much lower. Horse hyperimmune serum against rough S. typhimurium protects mice against infection with unrelated virulent smooth K. pneumoniae. Provided the Klebsiellae are preincubated in normal mouse serum bactericidal activity can also be demonstrated in vitro. This activity does not require the presence of complement and can be removed either by the same Klebsiella strain or by rough strains of Salmonellae but not by the smooth strain of Salmonellae from which these mutants originate. Although these effects would most easily be accounted for by specific antibodies it is also possible that they are instead attributable to a serum protein capable of charge interaction with rough antigens. In any event these findings, together with previous observations concerning degradation of somatic antigen and phenotypic modification of Klebsiellae recovered from endotoxin-treated mice, have led to the development of a new concept of natural immunity to Enterobacteriaceae. In this hypothesis, enzymatic factors capable of attacking cell wall components unmask R antigenic sites common to many bacterial strains and species. Thereafter the presence of a few types of "R" antibodies or of serum factors reacting with rough antigens have the capability of coping, like masterkeys, with a very wide range of infections due to serologically unrelated organisms.
Footnotes
1 Centre National de la Recherche Scientifique.
This article has been cited by other articles:
![]() |
J. Hellman, J. D. Roberts Jr., M. M. Tehan, J. E. Allaire, and H. S. Warren Bacterial Peptidoglycan-associated Lipoprotein Is Released into the Bloodstream in Gram-negative Sepsis and Causes Inflammation and Death in Mice J. Biol. Chem., April 12, 2002; 277(16): 14274 - 14280. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Th. Rietschel and J.-M. Cavaillon Endotoxin and anti-endotoxin The contribution of the schools of Koch and Pasteur: Life, milestone-experiments and concepts of Richard Pfeiffer (Berlin) and Alexandre Besredka (Paris) Innate Immunity, April 1, 2002; 8(2): 71 - 82. [PDF] |
||||
![]() |
J. Hellman and H. Shaw Warren Outer membrane protein A (OmpA), peptidoglycan-associated lipoprotein (PAL), and murein lipoprotein (MLP) are released in experimental Gram-negative sepsis Innate Immunity, February 1, 2001; 7(1): 69 - 72. [Abstract] [PDF] |
||||
![]() |
J. Hellman, P. M. Loiselle, M. M. Tehan, J. E. Allaire, L. A. Boyle, J. T. Kurnick, D. M. Andrews, K. Sik Kim, and H. S. Warren Outer Membrane Protein A, Peptidoglycan-Associated Lipoprotein, and Murein Lipoprotein Are Released by Escherichia coli Bacteria into Serum Infect. Immun., May 1, 2000; 68(5): 2566 - 2572. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Hellman and H. S. Warren Antibodies against bacterial membrane proteins Innate Immunity, August 1, 1999; 5(4): 213 - 215. [Abstract] [PDF] |
||||
![]() |
N. A. Nnalue All Accessible Epitopes in the Salmonella Lipopolysaccharide Core Are Associated with Branch Residues Infect. Immun., February 1, 1999; 67(2): 998 - 1003. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. A. Nnalue alpha -GlcNAc-1right-arrow2-alpha -Glc, the Salmonella Homologue of a Conserved Lipopolysaccharide Motif in the Enterobacteriaceae, Elicits Broadly Cross-Reactive Antibodies Infect. Immun., September 1, 1998; 66(9): 4389 - 4396. [Abstract] [Full Text] [PDF] |
||||
![]() |
S.E. Greisman and C.A. Johnston Review: Evidence against the hypothesis that antibodies to the inner core of lipopolysaccharides in antisera raised by immunization with enterobacterial deep-rough mutants confer broad-spectrum protection during Gram-negative bacterial sepsis Innate Immunity, April 1, 1997; 4(2): 123 - 153. [Abstract] [PDF] |
||||
![]() |
P.H. Lagrange, H.S. Blanchard, and A. Felten Review: Bacterial endotoxin and the human monoclonal antibody HA-IA: specificity, potential mechanisms of action, and limits to its effectiveness Innate Immunity, October 1, 1995; 2(5): 371 - 386. [Abstract] [PDF] |
||||
![]() |
A.S. Cross and S. Opal Minireview: Therapeutic intervention in sepsis with antibody to endotoxin: is there a future? Innate Immunity, March 1, 1994; 1(1): 57 - 69. [Abstract] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |