Session Information
AABB Annual Meeting & CTTXPO 2011
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The Role of the Innate Immune System in Blood Group Antigen Alloimmunization
Track : S - Scientific
Program Code: 9408-S
Date: Tuesday, October 25, 2011
Time: 10:30 AM to 12:00 PM  PST
Location: 30 A-C
DIRECTOR :
Dr. Christopher Tormey, MD, Associate Professor of Laboratory Medicine, Yale University School of Medicine
MODERATOR :
Dr. Christopher Tormey, MD, Associate Professor of Laboratory Medicine, Yale University School of Medicine
SPEAKER (S):
Stephanie Eisenbarth, MD, PhD, Assistant Professor
Interaction of Innate and Adaptive Immunity in Alloimmunization: An overview for Transfusion Medicine
Jeanne Hendrickson, MD, Assistant Professor, Emory University
RBC Alloimmunization: Lessons Learned from Murine Models
Eldad Hod, MD, Assistant Professor, Columbia University Medical Center
Description
The adaptive, humoral response to foreign antigens typically involves interactions between antigen-presenting cells, T cells and B cells resulting in alloantibody development. This is the classical model utilized by transfusion medicine physicians and scientists to explain alloimmunization to blood group antigens. Until recently, however, the intermediate processes by which antigen presentation induced T and B cell activation were poorly understood. Studies arising from basic immunology now suggest that components of the innate immune system, called pattern recognition receptors (PRRs), play an integral role in promoting T and B cell mediated responses. Innate PRR elements appear to "instruct" the adaptive, humoral arm of the immune system, thereby serving to initiate events that ultimately culminate in alloantibody formation. These exciting developments from the realm of basic immunology have many important implications for the field of transfusion medicine, and are particularly relevant to the induction of blood group alloantibodies following red cell exposure. Understanding the interaction between the innate and adaptive immune systems after transfusion may help to uncover the mechanisms underlying blood group alloimmunization. Moreover, such knowledge may allow transfusion medicine physicians and scientists to devise strategies to avoid provoking innate immunity and inducing an alloantibody response.

Jeanne Hendrickson did not give consent to be recorded or making presentation available






This session offers Self-Assessment Module (SAM) credit. Please complete the post test to receive SAM credit.

  • Compare evolving, state-of-the-art concepts regarding alloantibody formation resulting from interactions between innate and adaptive (including humoral) arms of the immune system.
  • Demonstrate how red blood cell antigens and surface alterations (eg, formation of advanced glycation end products) can mimic pathogen-associated molecular patterns to induce the innate immune system and promote the formation of blood group alloantibodies.
  • Discuss the accumulation of proinflammatory mediators (eg, iron) during red blood cell storage, and how such proinflammatory products may provoke the innate system to stimulate alloantibody development.


CE CategoryCE Value
California Clinical Laboratory Personnel 1.5
California Nurse 1.8
Florida Laboratory Personnel 1.8
General Attendee 1.5
Physician 1.5
Please note: Continuing education (CE) credit is available for online offerings only. Individuals that purchase CD-ROMs will not receive CE credit for the programs they view.


Handout Online
(Code: 9408-S)
List Price:Free
  
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