Mark R Wakefield

Dr. Mark R Wakefield

orcid

Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 October 2015 in Cancer Letters
Verified
Journal Article
Closed access
MMMark H. Mannino
Mark H. Mannino
ZZZiwen Zhu
Ziwen Zhu
HXHuaping Xiao
Huaping Xiao
QBQian Bai
Qian Bai
MWMark R Wakefield
Mark R Wakefield
YFYujiang Fang
Yujiang Fang

1 February 2007 in Seminars in Oncology
Verified
Journal Article
Closed access
JPJeffrey S. Palmgren
Jeffrey S. Palmgren
SKSaumil S. Karavadia
Saumil S. Karavadia
MWMark R Wakefield
Mark R Wakefield

1 April 2016 in Cancer Letters
Verified
Journal Article
Closed access
DXDixon H. Xu
Dixon H. Xu
ZZZiwen Zhu
Ziwen Zhu
MWMark R Wakefield
Mark R Wakefield
HXHuaping Xiao
Huaping Xiao
QBQian Bai
Qian Bai
YFYujiang Fang
Yujiang Fang

17 March 2017 in Anticancer Research
Verified
Journal Article
Closed access
PDF file
JLJack Lin
Jack Lin
ZZZiwen Zhu
Ziwen Zhu
HXHuaping Xiao
Huaping Xiao
MWMark R Wakefield
Mark R Wakefield
VDVivi A. Ding
Vivi A. Ding
YFYujiang Fang
Yujiang Fang
Interleukin-7 (IL-7) is a cytokine that has been known since long in immunology, mainly regarding its effects on T-cells and B-cells. IL-7 has been demonstrated to be necessary for both B-cell and T-cell proliferation and lack of IL-7 causes immature immune cell arrest. Interestingly, in recent years, certain studies have strongly suggested that the role of IL-7 is far beyond the field of immunology, it might have direct or indirect effect on cancer. This review aims to summarize the role of IL-7 in immunity and its role in the pathogenesis of neoplasia.

16 November 2010 in Clinical Transplantation
Verified
Journal Article
Closed access
PDF file
CRCynthia Russell
Cynthia Russell
VCVicki Conn
Vicki Conn
CACatherine Ashbaugh
Catherine Ashbaugh
RMRichard Madsen
Richard Madsen
MWMark R Wakefield
Mark R Wakefield
LPLeanne Peace
Leanne Peace

10 July 2019 in American Journal of Transplantation
Verified
Journal Article
Open access
PDF file
CRCynthia L. Russell
Cynthia L. Russell
DHDonna Hathaway
Donna Hathaway
LRLaura M. Remy
Laura M. Remy
DADana Aholt
Dana Aholt
DCDebra Clark
Debra Clark
KGKathy Goggin
Kathy Goggin
This study determined if a SystemCHANGE™ intervention was more efficacious than attention control in increasing immunosuppressive medication adherence and improving outcomes in adult kidney transplant recipients during a 6‐month intervention phase and subsequent 6‐month (no intervention) maintenance phase. The SystemCHANGE™ intervention taught patients to use person‐level quality improvement strategies to link adherence to established daily routines, environmental cues, and supportive people. Eighty‐nine patients (average age 51.8 years, 58% male, 61% African American) completed the 6‐month intervention phase. Using an intent‐to‐treat analysis, at 6 months, medication adherence for SystemCHANGE™ (median 0.91, IQR 0.76‐0.96) and attention control (median 0.67, IQR 0.52‐0.72) patients differed markedly (difference in medians 0.24, 95% CI 0.13‐0.30, P < .001). At the conclusion of the subsequent 6‐month maintenance phase, the gap between medication adherence for SystemCHANGE™ (median 0.77, IQR 0.56‐0.94) and attention control (median 0.60, IQR 0.44‐0.73) patients remained large (difference in medians 0.17, 95% CI 0.06‐0.33, P = .004). SystemCHANGE™ patients evidenced lower mean creatinine and BUN at 12 months and more infections at 6 and 12 months. This first fully powered RCT testing SystemCHANGE™ to improve and maintain medication adherence in kidney transplant recipients demonstrated large, clinically meaningful improvements in medication adherence. Clinical Trial Registration: NCT02416479.