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American journal of reproductive immunology (New York, N.Y. : 1989)1995; 33(3); 213-220; doi: 10.1111/j.1600-0897.1995.tb00887.x

An 80-kDa syncytiotrophoblast alloantigen bound to maternal alloantibody in term placenta.

Abstract: We have shown that most of the IgG present on term syncytiotrophoblast, membrane, microvesicles is bound to an 80 kDa protein antigen (R80K). Methods: Microvesicles were prepared from term human placenta, and the IgG eluted at pH3. Results: When IgG antibody was eluted at pH3 and reacted with acid-treated vesicles of other placentae, the alloantibody always bound to the preparation from which it was obtained, but only to about 10% of acid-treated preparations from other placentae. A similar polymorphic protein found in association with IgG antibody was found in term horse placentae. Cross-reactivity of the antibodies between species was not found. Using binding of labelled antibody, complement dependent cytotoxicity and FACS two-color analysis, the human polymorphic antigen was present on peripheral blood monocytes and B-lymphocytes. The R80k antigen on intact microvesicles was resistant to trypsin, but after acid elution of IgG, trypsin released a soluble 50 kDa fragment which reacted with the acid-eluted IgG antibody. Conclusions: The presence of antibodies to R80K in all term placentae studied, including first pregnancies, suggests that development of this alloantibody may be a normal requirement for successful pregnancy.
Publication Date: 1995-03-01 PubMed ID: 7546237DOI: 10.1111/j.1600-0897.1995.tb00887.xGoogle Scholar: Lookup
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  • Journal Article

Summary

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The research investigates an 80-kDa protein antigen found in the placenta at term, theorizing that the development of antibodies to this antigen may be crucial for a successful pregnancy. The researchers further discovered that this antigen is resistant to certain digestive enzymes and noted its presence in different blood cells.

Methodology

  • The researchers isolated microvesicles from term human placenta, and purposely adjusted the surrounding environment’s pH to a value of 3 to elute the IgG antibodies present.
  • These acid-eluted IgG antibodies were then reacted with acid-treated vesicles from other placentas.

Results

  • The alloantibody continually attached itself to the preparation it was originally obtained from, but reacted with only approximately 10% of the other placenta preparations treated with acid. This indicates a degree of specificity in the interaction between these antibodies and their original antigen sources.
  • They found a similar protein associated with IgG antibodies in term horse placentae, indicating potential similarities across species.
  • Despite these similarities, no cross-reactivity between the antibodies of different species was observed, indicating that the antibodies remain species-specific.
  • By using labeled antibodies and techniques such as complement dependent cytotoxicity and FACS two-color analysis, the researchers identified the presence of the human polymorphic antigen on peripheral blood monocytes and B-lymphocytes.
  • They found that the R80k antigen, present on intact microvesicles, was resistant to the digestion enzyme trypsin. However, after acid elution of IgG, trypsin was able to break down a soluble 50 kDa fragment, which still reacted with the acid-eluted IgG antibody. This suggests a level of protection the antigen offers to these antibodies.

Conclusions

  • The team concluded that the presence of antibodies to the R80K antigen in all the term placentae studied, including those from first pregnancies, implies that the development of this alloantibody may be a normal, and potentially essential, process for a successful pregnancy.

Cite This Article

APA
Jalali GR, Rezai A, Underwood JL, Mowbray JF, Surridge SH, Allen WR, Matthias S. (1995). An 80-kDa syncytiotrophoblast alloantigen bound to maternal alloantibody in term placenta. Am J Reprod Immunol, 33(3), 213-220. https://doi.org/10.1111/j.1600-0897.1995.tb00887.x

Publication

ISSN: 1046-7408
NlmUniqueID: 8912860
Country: Denmark
Language: English
Volume: 33
Issue: 3
Pages: 213-220

Researcher Affiliations

Jalali, G R
  • Department of Immunopathology, St. Mary's Hospital Medical School, London, England.
Rezai, A
    Underwood, J L
      Mowbray, J F
        Surridge, S H
          Allen, W R
            Matthias, S

              MeSH Terms

              • Animals
              • B-Lymphocytes / immunology
              • Binding Sites, Antibody
              • Cell Line, Transformed
              • Female
              • HLA Antigens / immunology
              • Herpesvirus 4, Human
              • Horses
              • Humans
              • Immunoglobulin G / immunology
              • Isoantibodies / immunology
              • Isoantigens / immunology
              • Isoantigens / isolation & purification
              • Male
              • Maternal-Fetal Exchange / immunology
              • Microbodies / immunology
              • Molecular Weight
              • Placenta / immunology
              • Pregnancy
              • T-Lymphocytes / immunology
              • Trophoblasts / immunology
              • Trypsin / pharmacology

              Citations

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