Lupus anticoagulants (LA) are immunoglobulins (IgG, IgM, IgA or a mixt
ure) which interfere with in vitro phospholipid (PL) dependent tests o
f coagulation (e.g. APTT, KCT, dilute Russell Viper Venom Time). LA ar
e heterogeneous; consequently, the laboratory diagnosis is difficult a
nd relies on multiple tests. We have developed a sensitive and relativ
ely specific confirmatory test system based on fractions of two snake
venoms. Textarin(R), 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 cofa
ctors. 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 popula
tions: LA positive, therapeutically heparinized, stable oral anticoagu
lated, liver disease, routine preoperative, anticardiolipin antibody p
ositive LA negative, hemophilia A, various other hereditary factor def
icien cies or dysfunctional proteins, and specific inhibitors of facto
r V and factor VIII. The LA positive patients represented a mixed popu
lation 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 effect
ively, it is recommended to incorporate polybrene with Textarin when e
valuating heparinized samples. Factor V deficiency and specific inhibi
tors of factor V yielded, in some instances, false positive results.