Literature DB >> 7690348

Determination of the specificities of monoclonal antibodies recognizing members of the CEA family using a panel of transfectants.

S Daniel1, G Nagel, J P Johnson, F M Lobo, M Hirn, P Jantscheff, M Kuroki, S von Kleist, F Grunert.   

Abstract

Carcinoembryonic antigen (CEA), one of the most clinically important tumor markers, is mainly used in the post-surgical surveillance of patients with colorectal carcinomas. CEA belongs to a large protein family, which includes cross-reacting antigens, e.g., non-specific cross-reacting antigens (NCAs) and biliary glycoprotein (BGP) as well as pregnancy-specific glycoproteins (PSGs). The genes encoding these proteins can be subdivided into the CEA and PSG subgroups. The members of the subgroups share antigenic determinants and show high similarity in amino-acid sequences. Their derived secondary structures show them to belong to the immunoglobulin superfamily. Due to the close relationship of the members of the CEA subgroup, it is very difficult to distinguish between the individual members with MAbs. Here we have used flow cytometric analysis of transfectants expressing individual members of the CEA subgroup as an alternative approach to determine the specificities of 13 MAbs. This allows us to examine the specificities of these antibodies for members of the CEA family, even of those which have not yet been characterized at the protein level. In addition, binding of the MAbs to NCAs expressed by polymorphonuclear cells (PMN) was tested by Western-blot analysis, immunoprecipitation and flow cytometry. Four antibodies bound exclusively to NCA-50/90 and one MAb (80H3) only to NCA-95. MAb 4/3/17 recognizes CEA and BGP on the surface of transfectants and NCA-160 from granulocytes. We assume that NCA-160 is a product of the BGP gene. On granulocytes, which do not express CEA, MAb 4/3/17 is specific for NCA-160 (BGP). Mutual inhibition of the MAbs binding to NCA-50/90 revealed 3 different epitope groups.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 7690348     DOI: 10.1002/ijc.2910550222

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  11 in total

1.  Differential recognition of members of the carcinoembryonic antigen family by Opa variants of Neisseria gonorrhoeae.

Authors:  M P Bos; F Grunert; R J Belland
Journal:  Infect Immun       Date:  1997-06       Impact factor: 3.441

2.  Functional activity of antibodies against the recombinant OpaJ protein from Neisseria meningitidis.

Authors:  M I de Jonge; G Vidarsson; H H van Dijken; P Hoogerhout; L van Alphen; J Dankert; P van der Ley
Journal:  Infect Immun       Date:  2003-05       Impact factor: 3.441

3.  Carcinoembryonic antigen family members CEACAM6 and CEACAM7 are differentially expressed in normal tissues and oppositely deregulated in hyperplastic colorectal polyps and early adenomas.

Authors:  S Schölzel; W Zimmermann; G Schwarzkopf; F Grunert; B Rogaczewski; J Thompson
Journal:  Am J Pathol       Date:  2000-02       Impact factor: 4.307

4.  A colonic tissue architecture assay applied to human colon carcinoma cells.

Authors:  C Ilantzis; C P Stanners
Journal:  In Vitro Cell Dev Biol Anim       Date:  1997-01       Impact factor: 2.416

5.  Carcinoembryonic antigen family receptor recognition by gonococcal Opa proteins requires distinct combinations of hypervariable Opa protein domains.

Authors:  Martine P Bos; David Kao; Daniel M Hogan; Christopher C R Grant; Robert J Belland
Journal:  Infect Immun       Date:  2002-04       Impact factor: 3.441

6.  Deregulated expression of the human tumor marker CEA and CEA family member CEACAM6 disrupts tissue architecture and blocks colonocyte differentiation.

Authors:  Christian Ilantzis; Luisa DeMarte; Robert A Screaton; Clifford P Stanners
Journal:  Neoplasia       Date:  2002 Mar-Apr       Impact factor: 5.715

7.  CD66 receptor specificity exhibited by neisserial Opa variants is controlled by protein determinants in CD66 N-domains.

Authors:  M P Bos; M Kuroki; A Krop-Watorek; D Hogan; R J Belland
Journal:  Proc Natl Acad Sci U S A       Date:  1998-08-04       Impact factor: 11.205

8.  Synthetic peptides from the N-domains of CEACAMs activate neutrophils.

Authors:  K M Skubitz; K D Campbell; A P Skubitz
Journal:  J Pept Res       Date:  2001-12

9.  Bacterial protein domains with a novel Ig-like fold target human CEACAM receptors.

Authors:  Nina M van Sorge; Daniel A Bonsor; Liwen Deng; Erik Lindahl; Verena Schmitt; Mykola Lyndin; Alexej Schmidt; Olof R Nilsson; Jaime Brizuela; Elena Boero; Eric J Sundberg; Jos A G van Strijp; Kelly S Doran; Bernhard B Singer; Gunnar Lindahl; Alex J McCarthy
Journal:  EMBO J       Date:  2021-02-01       Impact factor: 11.598

10.  A Diagnostic Analysis Workflow to Optimal Multiple Tumor Markers to Predict the Nonmetastatic Breast Cancer from Breast Lumps.

Authors:  Nan Jiang; Tian Tian; Xianyang Chen; Guofen Zhang; Lijie Pan; Chengping Yan; Guoshan Yang; Lili Wang; Xuchen Cao; Xin Wang
Journal:  J Oncol       Date:  2021-07-08       Impact factor: 4.375

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.