Abundant human anti-Galα3Gal antibodies display broad pathogen reactivity

被引:19
作者
Jensen, Jens Magnus Bernth [1 ]
Petersen, Mikkel Steen [1 ]
Ellerman-Eriksen, Svend [2 ]
Moller, Bjarne Kuno [1 ]
Jensenius, Jens Christian [3 ]
Sorensen, Uffe B. Skov [3 ]
Thiel, Steffen [3 ]
机构
[1] Aarhus Univ Hosp, Dept Clin Immunol, Aarhus, Denmark
[2] Aarhus Univ Hosp, Dept Clin Microbiol, Aarhus, Denmark
[3] Aarhus Univ, Dept Biomed, Aarhus, Denmark
关键词
NATURAL ANTI-GAL; ALPHA-1,3-GALACTOSYLTRANSFERASE GENE; IGG; IMMUNOGLOBULIN; POLYSACCHARIDE; ACTIVATION; BACTERIA;
D O I
10.1038/s41598-020-61632-9
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
Antibodies of the IgG class to terminal Gal alpha 3Gal (IgG anti-alpha Gal) is abundant in human plasma and are reported to bind most sepsis-causing Gram-negative bacteria. However, these seminal findings, made more than two decades ago, have not been reexamined. Our aim was to assess IgG anti-alpha Gal ' s pathogen reactivity. We affinity purified IgG anti-alpha Gal from a therapeutic grade normal human IgG pool applying two rounds of positive selection with Gal alpha 3Gal-coupled beads and included removal of column matrix reactive antibodies. The purified antibodies were rigorously characterized in terms of specificity and purity in various solid-phase immunoassays. We used flow cytometry to study reactivity against 100 consecutive clinical isolates diagnosed as cause of sepsis in humans. We found that the purified IgG anti-alpha Gal displays high specificity for Gal alpha 3Gal. Also, IgG anti-alpha Gal at 5mg/L bound 56 out of 100 pathogens with predilection for Gram-positive bacteria binding 39 out of 52 strains. We confirm that although IgG anti-alpha Gal comprise a small fraction of the human antibody pool (similar to 0.1%), these antibodies targets an impressively large part of pathogens causing invasive disease.
引用
收藏
页数:13
相关论文
共 30 条
[1]   STRUCTURAL STUDIES OF THE O-ANTIGENIC POLYSACCHARIDE OF ESCHERICHIA-COLI O86, WHICH POSSESSES BLOOD-GROUP-B ACTIVITY [J].
ANDERSSON, M ;
CARLIN, N ;
LEONTEIN, K ;
LINDQUIST, U ;
SLETTENGREN, K .
CARBOHYDRATE RESEARCH, 1989, 185 (02) :211-223
[2]   Natural anti-Gal antibodies constitute 0.2% of intravenous immunoglobulin and are equally retained on a synthetic disaccharide column or on an immobilized natural glycoprotein [J].
Barreau, N ;
Blancho, G ;
Boulet, C ;
Martineau, A ;
Vusio, P ;
Liaigre, J ;
Bovin, N ;
Bouhours, D ;
Bouhours, JF .
TRANSPLANTATION PROCEEDINGS, 2000, 32 (05) :882-883
[3]  
BARRETT DJ, 1986, CLIN EXP IMMUNOL, V63, P127
[4]   Biological variation of anti-αGal-antibodies studied by a novel Time-Resolved ImmunoFluorometric Assay [J].
Bernth-Jensen, Jens Magnus ;
Moller, Bjarne Kuno ;
Jensenius, Jens Christian ;
Thiel, Steffen .
JOURNAL OF IMMUNOLOGICAL METHODS, 2011, 373 (1-2) :26-35
[5]   QUANTITATIVE MEASURMENTS CONCERNING A AND B ANTIGEN SITES [J].
ECONOMID.J ;
HUGHESJO.NC ;
GARDNER, B .
VOX SANGUINIS, 1967, 12 (05) :321-&
[6]   THE HUMAN NATURAL ANTI-GAL IGG .3. THE SUBTLETY OF IMMUNE TOLERANCE IN MAN AS DEMONSTRATED BY CROSS-REACTIVITY BETWEEN NATURAL ANTI-GAL AND ANTI-B ANTIBODIES [J].
GALILI, U ;
BUEHLER, J ;
SHOHET, SB ;
MACHER, BA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1987, 165 (03) :693-704
[7]   A UNIQUE NATURAL HUMAN-IGG ANTIBODY WITH ANTI-ALPHA-GALACTOSYL SPECIFICITY [J].
GALILI, U ;
RACHMILEWITZ, EA ;
PELEG, A ;
FLECHNER, I .
JOURNAL OF EXPERIMENTAL MEDICINE, 1984, 160 (05) :1519-1531
[8]   EVOLUTIONARY RELATIONSHIP BETWEEN THE NATURAL ANTI-GAL ANTIBODY AND THE GAL-ALPHA-1-]3GAL EPITOPE IN PRIMATES [J].
GALILI, U ;
CLARK, MR ;
SHOHET, SB ;
BUEHLER, J ;
MACHER, BA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (05) :1369-1373
[9]   INTERACTION BETWEEN HUMAN NATURAL ANTI-ALPHA-GALACTOSYL IMMUNOGLOBULIN-G AND BACTERIA OF THE HUMAN FLORA [J].
GALILI, U ;
MANDRELL, RE ;
HAMADEH, RM ;
SHOHET, SB ;
GRIFFISS, JM .
INFECTION AND IMMUNITY, 1988, 56 (07) :1730-1737
[10]   ABO and Rh(D) phenotype frequencies of different racial/ethnic groups in the United States [J].
Garratty, G ;
Glynn, SA ;
McEntire, R .
TRANSFUSION, 2004, 44 (05) :703-706