Glycation of hemoglobin leads to the immunogenicity as a result of neo-epitope generation.

Abstract:

:Non-enzymatic glycation occurs rapidly which ultimately leads to the formation of advanced glycation endproducts (AGEs). These AGEs have shown to associated with the development of many diseases such as diabetes-mellitus. This study is focused on immunological characterization of glycated-Hb induced by d-ribose. Here, we analysed the immunogenicity of glycated-Hb by direct binding and competitive inhibition ELISA. Direct binding ELISA confirmed that glycated-Hb was highly immunogenic and induced high titre antibodies as compared to native-Hb. The antigen binding specificity and cross reactivity of these antibodies were also screened by competitive inhibition ELISA. The IgG from rabbit sera showed enhanced binding of glycated-Hb than native-Hb. Thus, it is possible that alterations in Hb induced by d-ribose could have generated highly immunogenic neoepitopes. Moreover, induced antibodies were also found to cross-react with other modified/native proteins. On the basis of the results of this study, we presume that this type of structural perturbations in Hb in vivo by d-ribose might take place in untreated diabetic condition that could induce such type of immunogenic auto-antibodies. Furthermore, increased level of these auto-antibodies could serve as a biomarker in diabetes and its progression.

journal_name

Int J Biol Macromol

authors

Siddiqui Z,Faisal M,Alatar AA,Ahmad S

doi

10.1016/j.ijbiomac.2018.11.063

subject

Has Abstract

pub_date

2019-02-15 00:00:00

pages

427-435

eissn

0141-8130

issn

1879-0003

pii

S0141-8130(18)34545-8

journal_volume

123

pub_type

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