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Routine monitoring for de novo DSA post-transplant: "Is the juice worth the squeeze?"
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Strategic development of antihumoral therapies provides a means for achieving enhanced therapeutic results. The basic immunobiology of humora alloresponses is currently adequate to allow development of new therapies. Plasma cell targeted therapy is one example of new treatment paradigms based on known immunobiology. This talk will describe the biologic basis for plasma cell targeting in general, and for proteasome inhibition in particular.
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