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B Dependency of a Late Anaphylactic Reaction
Address correspondence to Hern-Ku Lee, Dept. of Immunology, University National Medical School, Chonju, Chonbuk, 561-182, South Korea. Phone: 82-63-270-3069; Fax: 82-63-250-4215; E-mail: leeh-k{at}chonbuk.ac.kr
Anaphylaxis is a life-threatening systemic allergic reaction with the potential for a recurrent or biphasic pattern. Despite an incidence of biphasic reaction between 5 and 20%, the molecular mechanism for the reaction is unknown. Using a murine model of penicillin V–induced systemic anaphylaxis, we show an autoregulatory cascade of biphasic anaphylactic reactions. Induction of anaphylaxis caused a rapid increase in circulating platelet-activating factor (PAF) levels. In turn, the elevated PAF contributes to the early phase of anaphylaxis as well as the subsequent activation of the nuclear factor (NF)-
B, a crucial transcription factor regulating the expression of many proinflammatory cytokines and immunoregulatory molecules. The induction of NF-B activity is accompanied by TNF-
production, which, in turn, promotes late phase PAF synthesis. This secondary wave of PAF production leads eventually to the late phase of anaphylactic reactions. Mast cells do not appear to be required for development of the late phase anaphylaxis. Together, this work reveals the first mechanistic basis for biphasic anaphylactic reactions and provides possible therapeutic strategies for human anaphylaxis.
Key Words: early anaphylaxis • biphasic anaphylaxis • mast cell • penicillin V • TNF-
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