Literature DB >> 24010841

Natural antibodies to glycans.

N V Bovin1.   

Abstract

A wide variety of so-called natural antibodies (nAbs), i.e. immunoglobulins generated by B-1 cells, are directed to glycans. nAbs to glycans can be divided in three groups: 1) conservative nAbs, i.e. practically the same in all healthy donors with respect to their epitope specificity and level in blood; 2) allo-antibodies to blood group antigens; 3) plastic antibodies related to the first or the second group but discussed separately because their level changes considerably during diseases and some temporary conditions, in particular inflammation and pregnancy. Antibodies from the third group proved to be prospective markers of a number of diseases, whereas their unusual level (below or above the norm) is not necessarily the consequence of disease/state. Modern microarrays allowed the determination of the human repertoire, which proved to be unexpectedly broad. It was observed that the content of some nAbs reaches about 0.1% of total immunoglobulins. Immunoglobulins of M class dominate for most nAbs, constituting up to 80-90%. Their affinity (to a monovalent glycan, in KD terms) were found to be within the range 10(-4)-10(-6) M. Antibodies to Galβ1-3GlcNAc (Le(C)), 4-HSO3Galβ1-4GalNAc (4'-O-SuLN), Fucα1-3GlcNAc, Fucα1-4GlcNAc, GalNAcα1-3Gal (Adi), Galα1-4Galβ1-4Glc (P(k)), Galα1-4Galβ1-4GlcNAc (P1), GlcNAcα-terminated glycans, and hyaluronic acid should be noted among the nAbs revealed and studied during the last decade. At the same time, a kind of "taboo" is observed for a number of glycans: antibodies to Le(X) and Le(Y), and almost all gangliosides have not been observed in healthy persons. Many of the revealed nAbs were directed to constrained inner (core) part of glycan, directly adjoined to lipid of cell membrane or protein. The biological function of these nAbs remains unclear; for anti-core antibodies, a role of surveillance on appearance of aberrant, especially cancer, antigens is supposed. The first data related to oncodiagnostics based on quantitation of anti-glycan nAbs are reported.

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Year:  2013        PMID: 24010841     DOI: 10.1134/S0006297913070109

Source DB:  PubMed          Journal:  Biochemistry (Mosc)        ISSN: 0006-2979            Impact factor:   2.487


  15 in total

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3.  Immuno-PCR technology for detection of natural human antibodies against Lec disaccharide.

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Review 4.  Immunological Outcomes of Antibody Binding to Glycans Shared between Microorganisms and Mammals.

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6.  Blood Plasma-Derived Anti-Glycan Antibodies to Sialylated and Sulfated Glycans Identify Ovarian Cancer Patients.

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7.  A generalized quantitative antibody homeostasis model: antigen saturation, natural antibodies and a quantitative antibody network.

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9.  The glycosphingolipid P₁ is an ovarian cancer-associated carbohydrate antigen involved in migration.

Authors:  F Jacob; M Anugraham; T Pochechueva; B W C Tse; S Alam; R Guertler; N V Bovin; A Fedier; N F Hacker; M E Huflejt; N Packer; V A Heinzelmann-Schwarz
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10.  The Thomsen-Friedenreich Antigen-Specific Antibody Signatures in Patients with Breast Cancer.

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