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Blood, 1 February 2004, Vol. 103, No. 3, pp. 1099-1104.
Prepublished online as a Blood First Edition Paper on September 25, 2003; DOI 10.1182/blood-2003-04-1069.


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PHAGOCYTES

Granzyme B and perforin: constitutive expression in human polymorphonuclear neutrophils

Christof Wagner, Christof Iking-Konert, Birgit Denefleh, Sabine Stegmaier, Friederike Hug, and G. Maria Hänsch

From the Institut für Immunologie der Universität Heidelberg, Germany.

Polymorphonuclear neutrophils (PMNs) produce an abundance of bactericidal and cytotoxic molecules consistent with their role as first-line defense against bacterial infection. PMNs, however, also cause efficient cellular cytotoxicity when targeted through Fc receptors to appropriate antibody-coated target cells. Although this so-called antibody-dependent cellular cytotoxicity (ADCC) was described many years ago, the mechanism of killing is still elusive. We now have found that PMNs contain perforin and granzyme B, the 2 molecules known as the cytotoxic entity of natural killer cells and of cytotoxic T lymphocytes as well. Lysates of PMNs were lytic for chicken erythrocytes in a time-, temperature-, and Ca2+-dependent manner. Moreover, apoptosis of Jurkat cells was induced, consistent with the observation that the PMN lysates contain enzymatically active granzyme B. Taken together, our data provide evidence for the presence of perforin and granzyme B within the cytotoxic arsenal of PMNs. (Blood. 2004;103:1099-1104)


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Related Letters in Blood Online:

Granzyme A: an additional weapon of human polymorphonuclear neutrophils (PMNs) in innate immunity?
Kathrin Hochegger, Philipp Eller, and Alexander R. Rosenkranz
Blood 2004 103: 1176. [Full Text] [PDF]

Human neutrophils lack granzyme A, granzyme B, and perforin
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Blood 2004 104: 905-906. [Full Text] [PDF]



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