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Open AccessJournal ArticleDOI

Characteristics of an immune system common to certain external secretions

TLDR
The γ1A present in saliva and colostrum exists largely in the form of higher polymers, the major component of which has a sedimentation coefficient of 11S, and its properties including the local production of a distinctive type of antibody separate it from the "systemic" system responsible for the production of circulating antibody.
Abstract
The γ1A present in saliva and colostrum exists largely in the form of higher polymers, the major component of which has a sedimentation coefficient of 11S. The 11S γ1A in these fluids differs from the polymers found in normal and myeloma sera both immunologically and by the fact that their sedimentation coefficients are unaffected by disulfide bond reduction in the absence of urea. However, like other γ-globulins the 11S γ1A molecules consist of multiple polypeptide chains linked by disulfide bonds. Local synthesis of γ1A in the salivary gland has been shown by fluorescent and autoradiographic studies, although the fraction of the total salivary γ1A which is derived from local production is uncertain. No evidence of transport of intravenously administered I131-labeled 7S γ1A from serum to saliva was obtained. Immunological specificity has been demonstrated in the salivary and colostral γ1A. Whether that portion of the γ1A which is immunologically specific is a piece incorporated during the local synthesis of γ1A in the gland or is added by the epithelial cell in the process of transport remains to be determined. Antibody activity (isohemagglutinins) have been demonstrated in saliva and colostrum and have been shown to be of the γ1A-type. In both of these fluids activity is associated primarily with γ1A-polymers of 11S and 18S sizes. There appears to be an immunological system which is characteristic of certain external secretions. Its properties including the local production of a distinctive type of antibody separate it from the "systemic" system responsible for the production of circulating antibody. This system may play a significant role in the body's defense mechanisms against allergens and microorganisms.

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Journal ArticleDOI

Immunoglobulin A (IgA) Polymerization Sites in Human Immunocytes: Immunoelectron Microscopic Study

TL;DR: Investigating the cytoplasmic affinity of polymeric IgA for secretory component (SC) and the expression of joining (J) chain in pokeweek mitogen-stimulated human peripheral blood lymphocytes revealed that polymerization of human IgA and the addition of J chain occur in the perinuclear space and endoplasmic reticulum, prior to immunoglobulin secretion.
Book ChapterDOI

Enteric infection and immunization

TL;DR: Identification of IgA as a more specific marker of a ‘secretory immunoglobulin system’ by Tomasi et al. in 1965 stimulated a renewed interest in the local immune response and provided impetus to reopen the search for local vaccines to enhance mucosal resistance.
Journal ArticleDOI

Measuring the interaction of human secretory glycoproteins with oral bacteria.

TL;DR: Interactions of serous-type and submaxillary-type glycoproteins with oral bacteria are of biological interest equal to that of the reactions of antibodies, but commercial immunological reagents are unavailable for these glycoproteinins.
References
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Journal ArticleDOI

The thiobarbituric acid assay of sialic acids.

TL;DR: This chapter discusses the different aspects of thiobarbituric acid assay of sialic acid, which is suitable for measuring the release of bound sialoic acid by sialidase and hydrolysis of sIALic acid-containing material must be carried out for the measurement of total sialsic acids.
Journal ArticleDOI

Efficient trace-labelling of proteins with iodine.

TL;DR: Values greater than 50 per cent can be obtained by adding oxidizing agents to liberate iodine from iodide, but most if not all of these appear to affect adversely the properties of the labelled protein.
Journal ArticleDOI

Localization of antigen in tissue cells ii. improvements in a method for the detection of antigen by means of fluorescent antibody

TL;DR: Improvements in a method for the specific microscopic localization of antigen in tissue cells are described and two isomeric series derived from nitrofluorescein are described.
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