Glycans in immune recognition and response

被引:93
作者
Amon, Ron [1 ]
Reuven, Eliran Moshe [1 ]
Ben-Arye, Shani Leviatan [1 ]
Padler-Karavani, Vered [1 ]
机构
[1] Tel Aviv Univ, Dept Cell Res & Immunol, George S Wise Fac Life Sci, IL-69978 Tel Aviv, Israel
关键词
Sialic acid; Neu5Gc; Antibodies; Cancer; Immunotherapy; Biomarker; N-GLYCOLYLNEURAMINIC ACID; HANGANUTZIU-DEICHER ANTIGEN; NONHUMAN SIALIC-ACID; HUMAN XENO-AUTOANTIBODIES; VERTEBRATE AMINO-SUGARS; CELL LUNG-CANCER; CONTAINING GANGLIOSIDES; BREAST-CANCER; ALPHA-GAL; CHEMOENZYMATIC SYNTHESIS;
D O I
10.1016/j.carres.2014.02.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Glycans at the forefront of cells facilitate immune recognition processes. Cancer cells commonly present altered cell surface glycosylation, especially manifested in the expression of sialic acid at the termini of glycolipids and glycoproteins. Although tumor-associated carbohydrate antigens (TACAs) result in expression of altered-self, most such carbohydrates do not elicit strong humoral responses. Various strategies had been devised to elicit increased immunogenicity of such TACA aiming for potent immunotherapeutic antibodies or cancer vaccines. However some carbohydrates are immunogenic in humans and hold potential for novel glycotherapies. N-Glycolylneuraminic acid (Neu5Gc) is a foreign immunogenic sugar in humans originating from the diet (e.g., red meat) and subsequently expressed on the cell surface, especially accumulating on carcinoma. Consequently, the human immune system detects this non-self carbohydrate generating a broad anti-Neu5Gc antibody response. The co-existence of Neu5Gc/anti-Neu5Gc within humans spurs chronic inflammation mediated disease, including cancer. Concurrently, anti-Neu5Gc antibodies hold potential for novel targeted therapy. alpha Gal is another foreign immunogenic carbohydrate antigen in humans and all humans have circulating anti-Gal antibodies. This review aims to describe the immunogenicity of Neu5Gc and its implications for human diseases, highlighting differences and similarities with aGal and its potential for novel targeted theranostics. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:115 / 122
页数:8
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