Abstract #6 - P-19: Expansion Differentiation and Selection of B Cell Clones in Rejected Kidney Grafts

Feb 15, 2013 6:35pm ‐ Feb 15, 2013 6:38pm

Identification: FR13g


Abstract #7 - P-45: Use of Bortezomib to Successfully Treat Antibody-mediated Rejection (ABMR) in Intestinal Transplantation

Feb 15, 2013 6:38pm ‐ Feb 15, 2013 6:41pm

Identification: FR13h


Abstract #8 - P-03: Costimulation Blockade Prevents Antibody-mediated Rejection via Follicular Helper T Cell Modulation in Nonhuman Primate Renal Transplantation

Feb 15, 2013 6:41pm ‐ Feb 15, 2013 6:44pm

Identification: FR13i


The Natural Course of Antibody-mediated Allograft Injury

Feb 16, 2013 8:00am ‐ Feb 16, 2013 8:30am

Identification: SA01

Routine monitoring for de novo DSA post-transplant: "Is the juice worth the squeeze?"

What You'll Take Away from His Talk:

  • Understand the natural history of de novo HLA antibody in low risk patients.
  • Understand the patient phenotypes associated with de novo HLA antibodies post-transplant.
  • Understand the risk factors associated with de novo HLA antibodies.

Chronic Antibody-mediated Rejection: With and Without C4d

Feb 16, 2013 8:30am ‐ Feb 16, 2013 9:00am

Identification: SA02


Antibody, Tolerance, and Accommodation

Feb 16, 2013 9:30am ‐ Feb 16, 2013 10:00am

Identification: SA04


IVIG with and without Anti-B Cell Targeting (Desensitization and Therapy)

Feb 16, 2013 10:30am ‐ Feb 16, 2013 11:00am

Identification: SA05

I will be discussing current methods for desensitization as well as ongoing clinical trials we are conducting. Currently, there are several unresolved controversies and questions regarding the efficacy and economics of desensitization. I will address these and hopefully help clarify some of the outstanding controversies. I would hope that the audience would come away with a better understanding of the options and opportunities for transplantation that are created by desensitization. Also, what the future holds and how to refine desensitization protocols to insure the appropriate patients are treated and parameters for choosing an appropriate kidney for each patient are clearly defined.

Is There a Role for Bortezomib?

Feb 16, 2013 11:00am ‐ Feb 16, 2013 11:30am

Identification: SA06

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.

What You'll Take Away from His Talk:

  • Substantial evidence exists from basic research that plasma cell targeted therapy may provide a viable means for mitigating humoral alloresponses.
  • Initial evidence from clinical experiences with proteasome inhibition indicate that proteasome inhibitor-based regimens offer therapeutic potential.
  • Substantial opportunities exist for enhancing proteasome inhibitor therapy via combinatorial strategies.

Anti-C5 Therapy and No PLEX

Feb 16, 2013 11:30am ‐ Feb 16, 2013 12:00pm

Identification: SA07


Combination Therapies in Acute and Chronic-active AMR

Feb 16, 2013 12:00pm ‐ Feb 16, 2013 12:30pm

Identification: SA08