Literature DB >> 6967453

Influence of carrier-specific, thymus-derived cells on the immunologlobulin M antibody response to staphylococcal lipoteichoic acid.

P R Beining, G M Flannery, B Prescott, P J Baker.   

Abstract

The immunoglobulin M antibody response to the lipoteichoic acid (LTA) of Staphylococcus aureus ATCC 6538P was examined by a procedure in which erythrocytes sensitized with periodate-activated LTA were used for the detection of immunoglobulin M-producing plaque-forming cells LTA-specific plaque-forming cells were first detected 2 days after immunization with heat-killed bacterial cells, and maximal numbers of plaque-forming cells, mostly of the immunoglobulin M class rather than the immunoblogulin G or immunoglobulin A class, were attained by day 4; specificity for LTA was affirmed by plaque inhibition tests. No plaque-forming cells were found in mice given isolated LTA over a 10,000-fold range of immunizing doses. Mice pretreated with a carrier known to activate thymus-derived helper lymphocytes produced a plaque-forming cell response to LTA only when immunized with LTA bound to the same carrier. This suggests that carrier-specific thymus-derived cells are needed to initiate an antibody response to poorly immunogenic LTA. Since an antibody response can be elicited in mice given heat-killed cells, other cell wall and/or cell membrane constituents may play an important role as immunologically active carriers for this antigen.

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Year:  1980        PMID: 6967453      PMCID: PMC551085          DOI: 10.1128/iai.29.1.132-139.1980

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  35 in total

1.  Methods for coupling protein or polysaccharide to red cells by periodate oxidation.

Authors:  C J Sanderson; D V Wilson
Journal:  Immunochemistry       Date:  1971-02

2.  Characterization of the antibody response to type 3 pneumococcal polysaccharide at the cellular level. I. Dose-response studies and the effect of prior immunization on the magnitude of the antibody response.

Authors:  P J Baker; P W Stashak; D F Amsbaugh; B Prescott
Journal:  Immunology       Date:  1971-04       Impact factor: 7.397

3.  Characterization of the antibody response to type 3 pneumococcal polysaccharide at the cellular level. 3. Studies on the average avidity of the antibody produced by specific plaque-forming cells.

Authors:  P J Baker; B Prescott; P W Stashak; D F Amsbaugh
Journal:  J Immunol       Date:  1971-09       Impact factor: 5.422

4.  Studies on the group F antigen of lactobacilli: detection of antibodies by haemagglutination.

Authors:  M J Hewett; K W Knox; A J Wicken
Journal:  J Gen Microbiol       Date:  1970-03

5.  Regulatory role of T cells in IgG antibody formation and immune memory to type III Pneumococcal polysaccharide.

Authors:  H Braley-Mullen
Journal:  J Immunol       Date:  1974-12       Impact factor: 5.422

6.  Extraction and purification of lipoteichoic acids from Gram-positive bacteria.

Authors:  J Coley; M Duckworth; J Baddiley
Journal:  Carbohydr Res       Date:  1975-03       Impact factor: 2.104

7.  The glycerol teichoic acid of walls of Staphylococcus lactis I3.

Authors:  A R Archibald; J Baddiley; D Button
Journal:  Biochem J       Date:  1968-12       Impact factor: 3.857

8.  The lipid-teichoic acid complex in the cytoplasmic membrane of Streptococcus faecalis N.C.I.B. 8191.

Authors:  P Toon; P E Brown; J Baddiley
Journal:  Biochem J       Date:  1972-04       Impact factor: 3.857

9.  Lipoteichoic acid localization in mesosomal vesicles of Staphylococcus aureus.

Authors:  E Huff; R M Cole; T S Theodore
Journal:  J Bacteriol       Date:  1974-10       Impact factor: 3.490

10.  Synthesis of two classes of antibody, gammaM and gammaG or gammaM and gammaA, by identical cells. Amplification of the antibody response to pneumococcal polysaccharide type III.

Authors:  V J Pasanen; R Asofsky; P J Baker
Journal:  J Exp Med       Date:  1979-05-01       Impact factor: 14.307

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  2 in total

1.  Detection and specificity of antibodies secreted by spleen cells in mice immunized with Streptococcus mutans.

Authors:  M W Russell; C Czerkinsky; Z Moldoveanu
Journal:  Infect Immun       Date:  1986-08       Impact factor: 3.441

2.  Immune response of neonates to pneumococcal polysaccharide-protein conjugate.

Authors:  K T Lin; C J Lee
Journal:  Immunology       Date:  1982-06       Impact factor: 7.397

  2 in total

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