alexa The Role of Complement System in Graft versus Host Dise
ISSN: 2155-9864

Journal of Blood Disorders & Transfusion
Open Access

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Research Article

The Role of Complement System in Graft versus Host Disease

Mohamad A Cherry1, Hiral Parekh1, Megan Lerner2, Zhongxin Yu3, Sarah K Vesely4, George Selby1 and Jennifer Holter1,5*

1Division of Hematology and Oncology, University Health Sciences Center (OUHSC), Oklahoma City, OK, USA

2Department of Surgery, University Health Sciences Center (OUHSC), Oklahoma City, OK, USA

3Department of Pathology, University Health Sciences Center (OUHSC), Oklahoma City, OK, USA

4Department of Biostatistics and Epidemiology, College of Public Health Oklahoma, USA

5Department of Radiation Oncology, University Health Sciences Center (OUHSC), Oklahoma City, OK, USA

Corresponding Author:
Jennifer Holter, MD
The Oklahoma University Stephenson Cancer Center
Oklahoma City, OK 73104, USA
Tel: 405-271-4022
Fax: 405-271-4221
E-mail: [email protected]

Received Date: March 31, 2015; Accepted Date: April 25, 2015; Published Date: April 30, 2015

Citation: Cherry MA, Parekh H, Lerner M, Yu Z, Vesely SK, et al. (2015) The Role of Complement System in Graft versus Host Disease. J Blood Disord Transfus 6:274. doi: 10.4172/2155-9864.1000274

Copyright: © 2015 Cherry MA, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

 

Abstract

The role of complement system in stem cell transplantation is largely unknown. In solid organ transplantation, endovascular C4d deposition, a degradation product of the classic complement pathway, is essential for early rejection diagnosis. We retrospectively analyzed all patients diagnosed with graft versus host disease (GVHD) for C4d deposition at Oklahoma University between years 2000 and 2008. A modified Banff07 grading system was used to quantify C4d deposition. 58 biopsies (40 skin, 18 colon) performed on patients clinically suspected of having GVHD and 12 controls (all colon biopsies) were analyzed for C4d deposition. We recorded “response to steroids” in all clinical GVHD cases and looked at whether C4d can be utilized as a predictor of steroid treatment response. Of 40 clinical skin GVHD cases, 27 showed positive C4d staining which did not correlate well with steroid sensitivity: 74% of positive C4d cases responded to steroid therapy compared to 92% for negative cases (p=0.2634). 94% of colon GVHD cases showed positive C4d staining compared to 17% in controls (p<0.001). Only 44% of clinical colon GVHD cases were confirmed pathologically by H&E, compared to 93% of skin GVHD cases. For colon GVHD cases, 61% had clinical grade III/IV, and 78% responded to steroids. Interestingly, 90% of negative H&E colon cases responded to steroids. In conclusion, C4d deposition is a valuable marker for detection of colon GVHD, indicating a potential role of complement system in the pathogenesis of GVHD. C4d staining is potentially an objective tool than can help pathologist, in addition to H&E, to diagnosed colon GVHD.

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