Abstract
The anti-platelet activity of horse sera raised against human peripheral or thoracic duct lymphocytes was measured by three methods, platelet agglutination, clot retraction and the lowering of the electrophoretic mobility of platelets. The last method proved the most sensitive by a factor of at least 10. No activity was detected in antisera raised against thoracic duct cells, whereas all antisera against peripheral cells had significant titres. The source of the antigen responsible is discussed.
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