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Tytuł pozycji:

The role of immunity in the pathogenesis of experimental hematogenous pyelonephritis.

Tytuł:
The role of immunity in the pathogenesis of experimental hematogenous pyelonephritis.
Autorzy:
SANFORD JP
HUNTER BW
SOUDA LL
Źródło:
The Journal of experimental medicine [J Exp Med] 1962 Feb 01; Vol. 115, pp. 383-410.
Typ publikacji:
Journal Article
Język:
English
Imprint Name(s):
Original Publication: New York, NY : Rockefeller University Press
MeSH Terms:
Escherichia coli*
Immune Sera*
Klebsiella Infections*
Klebsiella pneumoniae*
Proteus mirabilis*
Pyelonephritis/*immunology
Animals ; Rabbits ; Rats
References:
J Exp Med. 1956 Sep 1;104(3):383-409. (PMID: 13357692)
Br Med J. 1945 Mar 17;1(4393):366-8. (PMID: 20785960)
J Exp Med. 1956 Jul 1;104(1):53-65. (PMID: 13332180)
J Exp Med. 1961 Sep 1;114:327-42. (PMID: 13702952)
Proc Soc Exp Biol Med. 1961 Jun;107:402-4. (PMID: 13773738)
Bull N Y Acad Med. 1961 Jul;37(7):448-67. (PMID: 19312678)
J Immunol. 1957 May;78(5):387-94. (PMID: 13449328)
J Urol. 1955 Nov;74(5):674-82. (PMID: 13272281)
J Urol. 1957 Nov;78(5):532-9. (PMID: 13476527)
J Exp Med. 1961 Sep 1;114:375-84. (PMID: 13683129)
Ann Surg. 1956 Jul;144(1):51-6. (PMID: 13327841)
J Immunol. 1955 Jun;74(6):466-78. (PMID: 14392332)
J Infect Dis. 1955 Jul-Aug;97(1):57-65. (PMID: 13242854)
J Exp Med. 1959 Nov 1;110:685-97. (PMID: 13798253)
J Clin Invest. 1955 Oct;34(10):1489-97. (PMID: 13263428)
Contributed Indexing:
Keywords: PYELONEPHRITIS/immunology*
Substance Nomenclature:
0 (Immune Sera)
Entry Date(s):
Date Created: 19620201 Date Completed: 19981101 Latest Revision: 20190509
Update Code:
20240104
PubMed Central ID:
PMC2137485
DOI:
10.1084/jem.115.2.383
PMID:
14496914
Czasopismo naukowe
Hematogenous pyelonephritis was produced in rats utilizing multiple strains of Escherichia coli, a strain of Klebsiella pneumoniae, and a strain of Proteus mirabilis. Three patterns of hematogenous pyelonephritis occurred which represent an interrelationship between an immune response to the infecting bacteria and the development of obstructive uropathy as a consequence of infection. First, the course of pyelonephritis due to strains of Escherichia coli was acute, self-limited, and associated with the development of circulating agglutinins. Following healing, this pattern of infection was associated with acquired resistance to reinfection with the same bacterial strain. Second, the course of pyelonephritis due to a strain of Klebsiella pneumoniae type C was chronic. This infection was not associated with the production of circulating agglutinins against encapsulated strains. Acquired resistance to reinfection by the homotypic strain could not be demonstrated following eradication of infection but was produced by the passive transfer of concentrated antiserum. Third, pyelonephritis due to Proteus mirabilis was associated with circulating agglutinins and resistance to reinfection with the same organism following eradication of infection, yet the course was chronic. The chronicity appeared to be the consequence of obstructive uropathy resulting from calculi which developed during the course of the infection. Resistance to reinfection was demonstrated in infections with strains of E. coli and P. mirabilis. The resistance is associated with specific immunity as demonstrated by the observation that: (a) it is type-specific, (b) it is of at least 3 months' duration, and (c) it can be passively transferred by means of rabbit antiserum. Since K. pneumoniae failed to evoke capsular antibodies in the rat, resistance to infection with K. pneumoniae was produced only by means of passively transferred concentrated rabbit antiserum and not by prior infection. Immunity can be demonstrated to have a significant role in the pathogenesis of experimental hematogenous pyelonephritis only in the absence of obstructive uropathy.

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