Lupus
anticoagulants (LA) are
immunoglobulins (
IgG,
IgM,
IgA or a mixture) which interfere with in vitro phospholipid (PL) dependent tests of coagulation (e.g. APTT, KCT, dilute Russell Viper Venom Time). LA are heterogeneous; consequently, the laboratory diagnosis is difficult and relies on multiple tests. We have developed a sensitive and relatively specific confirmatory test system based on fractions of two
snake venoms.
Textarin,
a protein fraction of Pseudonaja textilis
venom (Australian Eastern brown snake), activates
prothrombin in the presence of PL,
factor V and
calcium ions.
Ecarin,
a protein fraction of Echis carinatus
venom, will activate
prothrombin in the absence of any cofactors. The activation of
prothrombin by
Textarin yields
thrombin while
Ecarin yields
meizothrombin. In the presence of LA, the
Textarin time is prolonged and the
Ecarin time is unaffected. The test results are reported as a ratio of
Textarin/
Ecarin times (abnormal greater than 1.3). We have evaluated this test system in the following patient populations: LA positive, therapeutically heparinized, stable oral anticoagulated,
liver disease, routine preoperative,
anticardiolipin antibody positive LA negative,
hemophilia A, various other hereditary factor deficiencies or dysfunctional
proteins, and specific inhibitors of
factor V and
factor VIII. The LA positive patients represented a mixed population of
autoimmune disease, drug-induced and post-infectious states. Our findings indicate the sensitivity of the
Textarin/
Ecarin system in the confirmation of LA. In order to use the test system most effectively, it is recommended to incorporate
polybrene with
Textarin when evaluating heparinized samples.
Factor V deficiency and specific inhibitors of
factor V yielded, in some instances, false positive results.