Thromb Haemost 1996; 75(02): 303-308
DOI: 10.1055/s-0038-1650265
Original Article
Schattauer GmbH Stuttgart

Anticardiolipin and Anti-β2-GPI Are Two Distinct Populations of Autoantibodies

M Sorice
The Dipartimento di Medicina Sperimentale, Universita “La Sapienza”, Rome, Italy
,
A Circella
The Dipartimento di Medicina Sperimentale, Universita “La Sapienza”, Rome, Italy
,
T Griggi
The Dipartimento di Medicina Sperimentale, Universita “La Sapienza”, Rome, Italy
,
T Garofalo
The Dipartimento di Medicina Sperimentale, Universita “La Sapienza”, Rome, Italy
,
G Nicodemo
The Dipartimento di Medicina Sperimentale, Universita “La Sapienza”, Rome, Italy
,
V Pittoni
1   Clinica Medica I, Universita “La Sapienza”, Rome, Italy
,
G M Pontieri
The Dipartimento di Medicina Sperimentale, Universita “La Sapienza”, Rome, Italy
,
L Lenti
The Dipartimento di Medicina Sperimentale, Universita “La Sapienza”, Rome, Italy
,
G Valesini
1   Clinica Medica I, Universita “La Sapienza”, Rome, Italy
› Author Affiliations
Further Information

Publication History

Received: 03 August 1995

Accepted after revision06 November 1995

Publication Date:
31 August 2018 (online)

Summary

This study has been undertaken to assess whether anticardiolipin and anti-(32-GPI are two distinct populations of (auto)antibodies, and to clarify whether the β2-GPI region critical for phospholipid binding is also crucial for anti-β2-GPI reactivity.

Fourteen of the 62 anticardiolipin (aCL) ELISA positive sera (22.6%) were positive for anti-β2-GPI by immunoblotting, 42 (67.7%) for aCL using TLC immunostaining.

IgG fractions from 5 sera gave the same anticardiolipin reactivity detected by TLC immunostaining in the corresponding sera.

All anti-β2-GPI-positive sera were reactive with the phenylthio-carbamyl derivative of the protein, indicating that binding of phe-nylisothiocyanate with lysine residues does not modify the molecule antigenicity. In addition, incubation of IgG fractions with the phospholipid binding site did not modify reactivity with β2-GPI.

These findings demonstrate that: a) “true” antiphospholipid antibodies are detectable in patients sera; b) aCL and anti-β2-GPI have a different immunological profile; c) the β2-GPI phospholipid-binding site is not the region recognized by the antibodies.

 
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