Unique repertoire of anti-carbohydrate antibodies in individual human serum

被引:29
作者
Luetscher, Ralph N. D. [1 ,5 ]
McKitrick, Tanya R. [1 ]
Gao, Chao [1 ]
Mehta, Akul Y. [1 ]
McQuillan, Alyssa M. [1 ]
Kardish, Robert [1 ,6 ]
Boligan, Kayluz Frias [2 ]
Song, Xuezheng [3 ]
Lu, Lenette [4 ,7 ]
Heimburg-Molinaro, Jamie [1 ]
von Gunten, Stephan [2 ]
Alter, Galit [4 ]
Cummings, Richard D. [1 ]
机构
[1] Harvard Med Sch, Dept Surg, Beth Israel Deaconess Med Ctr, Natl Ctr Funct Glyc, CLS 11087 3 Blackfan Circle, Boston, MA 02115 USA
[2] Univ Bern, Inst Pharmacol, CH-3010 Bern, Switzerland
[3] Emory Univ, Sch Med, Dept Biochem, Atlanta, GA 30303 USA
[4] Ragon Inst MGH MIT & Harvard, Cambridge, MA 02139 USA
[5] Swiss Fed Inst Technol, Inst Microbiol, Dept Biol, CH-8093 Zurich, Switzerland
[6] Scien US, 2640 West Medtron Way, Tempe, AZ 85281 USA
[7] UT Southwestern Med Ctr, Div Infect Dis & Geog Med, Dept Internal Med, 5323 Harry Hines Blvd, Dallas, TX 75390 USA
基金
瑞士国家科学基金会; 美国国家卫生研究院;
关键词
SCHISTOSOMA-MANSONI SYNTHESIZES; INFLUENZAE TYPE-B; ABO BLOOD-GROUP; LINKED OLIGOSACCHARIDES; FUCOSYLATED LACDINAC; HELICOBACTER-PYLORI; MICROARRAY STRATEGY; GLYCAN MICROARRAYS; NATURAL ANTIBODIES; CARBOHYDRATE;
D O I
10.1038/s41598-020-71967-y
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Humoral immunity to pathogens and other environmental challenges is paramount to maintain normal health, and individuals lacking or unable to make antibodies are at risk. Recent studies indicate that many human protective antibodies are against carbohydrate antigens; however, little is known about repertoires and individual variation of anti-carbohydrate antibodies in healthy individuals. Here we analyzed anti-carbohydrate antibody repertoires (ACARs) of 105 healthy individual adult donors, aged 20-60(+) from different ethnic backgrounds to explore variations in antibodies, as defined by binding to glycan microarrays and by affinity purification. Using microarrays that contained>1,000 glycans, including antigens from animal cells and microbes, we profiled the IgG and IgM ACARs from all donors. Each donor expressed many ACAs, but had a relatively unique ACAR, which included unanticipated antibodies to carbohydrate antigens not well studied, such as chitin oligosaccharides, Forssman-related antigens, globo-type antigens, and bacterial glycans. We also saw some expected antibodies to ABO(H) blood group and alpha-Gal-type antigens, although these also varied among individuals. Analysis suggests differences in ACARs are associated with ethnicity and age. Thus, each individual ACAR is relatively unique, suggesting that individualized information could be useful in precision medicine for predicting and monitoring immune health and resistance to disease.
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页数:15
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