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MAbs. 2017 Apr;9(3):567-577. doi: 10.1080/19420862.2017.1288770.

A new anti-mesothelin antibody targets selectively the membrane-associated form.

Author information

1
a University of Bourgogne-Franche-Comte , Besançon Cedex , France.
2
b ITAC Platform of Clinical Investigation Center-Biotherapy , Besançon Cedex , France.
3
c Blood Bank Bourgogne-Franche-comté , Porto , Portugal.
4
d Fairjourney Biologics , Porto , Portugal.
5
e J.Minjoz University Hospital , Besançon Cedex , France.
6
f arGEN-X BVBA , Zwijnaarde , Belgium.
7
g Mabdesigns , London , UK.

Abstract

Mesothelin is a glycosylphosphatidylinositol (GPI)-anchored membrane protein that shows promise as a target for antibody-directed cancer therapy. High levels of soluble forms of the antigen represent a barrier to directing therapy to cellular targets. The ability to develop antibodies that can selectively discriminate between membrane-bound and soluble conformations of a specific protein, and thus target only the membrane-associated antigen, is a substantive issue. We show that use of a tolerance protocol provides a route to such discrimination. Mice were tolerized with soluble mesothelin and a second round of immunizations was performed using mesothelin transfected P815 cells. RNA extracted from splenocytes was used in phage display to obtain mesothelin-specific antigen-binding fragments (Fabs) that were subsequently screened by flow cytometry and ELISA. This approach generated 147 different Fabs in 34 VH-CDR3 families. Utilizing competition assays with soluble protein and mesothelin-containing serum obtained from metastatic cancer patients, 10 of these 34 VH-CDR3 families were found to bind exclusively to the membrane-associated form of mesothelin. Epitope mapping performed for the 1H7 clone showed that it does not recognize GPI anchor. VH-CDR3 sequence analysis of all Fabs showed significant differences between Fabs selective for the membrane-associated form of the antigen and those that recognize both membrane bound and soluble forms. This work demonstrates the potential to generate an antibody specific to the membrane-bound form of mesothelin. 1H7 offers potential for therapeutic application against mesothelin-bearing tumors, which would be largely unaffected by the presence of the soluble antigen.

KEYWORDS:

Competition assay; membrane-specific antibody; mesothelin; phage display; serum mesothelin; soluble mesothelin; therapeutic antibody; tolerance immunization

PMID:
28353419
PMCID:
PMC5384705
DOI:
10.1080/19420862.2017.1288770
[Indexed for MEDLINE]
Free PMC Article

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