Decreased expression of programmed death-1 on CD8+ effector memory T lymphocytes correlates with the pathogenesis of type 1 diabetes

Author(s):  
Yimei Shan ◽  
Yinghong Kong ◽  
Yan Zhou ◽  
Jingjing Guo ◽  
Qiyun Shi ◽  
...  
2009 ◽  
Vol 83 (3) ◽  
pp. 289-294 ◽  
Author(s):  
Scherezade Momin ◽  
Sylvia Flores ◽  
Bárbara Angel B ◽  
Ethel Codner D ◽  
Elena Carrasco P ◽  
...  

2019 ◽  
Vol 203 (4) ◽  
pp. 844-852 ◽  
Author(s):  
Tijana Martinov ◽  
Linnea A. Swanson ◽  
Elise R. Breed ◽  
Christopher G. Tucker ◽  
Alexander J. Dwyer ◽  
...  

PLoS ONE ◽  
2014 ◽  
Vol 9 (2) ◽  
pp. e89561 ◽  
Author(s):  
Nora M. Kochupurakkal ◽  
Annie J. Kruger ◽  
Sudipta Tripathi ◽  
Bing Zhu ◽  
La Tonya Adams ◽  
...  

2010 ◽  
Vol 33 (11) ◽  
pp. 1825-1833 ◽  
Author(s):  
Tae Joon Won ◽  
Yu Jin Jung ◽  
Seok Joong Kwon ◽  
Yoon Jeong Lee ◽  
Do Ik Lee ◽  
...  

2020 ◽  
pp. 107815522092154
Author(s):  
Nikhila Kethireddy ◽  
Steffi Thomas ◽  
Poorva Bindal ◽  
Prateek Shukla ◽  
Upendra Hegde

Introduction Immune agents including anti-programmed death receptor-1 and anti-cytotoxic T-lymphocyte antigen-4 have been associated with numerous immune-related complications. Pembrolizumab, a programmed death-1 inhibitor, has been associated with a number of immune-related adverse events such as pneumonitis, colitis, hepatitis, hypophysitis, hyperthyroidism, hypothyroidism, nephritis, and type 1 diabetes. Case report We present a rare case of an elderly male on pembrolizumab who suffered from four autoimmune toxicities including type 1 diabetes, pneumonitis, hypothyroidism, and polymyalgia rheumatica likely catalyzed by age-related immune activation. Management and outcome: Immunotherapy was indefinitely stopped, and patient was started on steroids for the immune-related adverse events with complete resolution of polymyalgia rheumatica. Thyroid dysfunction resolved once he started thyroid replacement therapy. His diabetes is well controlled with insulin and is followed by endocrinology. He continues on prednisone for immune-mediated pneumonitis with a good response with regular monitoring via computed tomography scans and pulmonary consultation. Discussion Few cases wherein multiple toxicities are seen within one patient are reported. Aging appears to be a risk factor for immune-related adverse events. Aging is associated with an increased incidence of autoimmunity as programmed death-1 ligand expression represents an important mechanism that tissues use to protect from self-reactive effector T cells. Programmed death-1 blockade breaks this protective mechanism and enhances autoimmune diseases. Therefore, close monitoring and extreme vigilance is warranted while using immune checkpoint inhibitors including pembrolizumab as multiple toxicities can occur within a short span of infusion, especially in elderly individuals. Prompt discontinuation and the use of a multidisciplinary team are prudent to prevent further morbidity and mortality.


2017 ◽  
Vol 55 (5) ◽  
pp. 515-517 ◽  
Author(s):  
Xiaohong Chen ◽  
Heming Guo ◽  
Sicheng Li ◽  
Cuiping Liu ◽  
Sisi Ding ◽  
...  

2012 ◽  
Vol 188 (7) ◽  
pp. 3138-3149 ◽  
Author(s):  
Nadir Kadri ◽  
Eva Korpos ◽  
Shashank Gupta ◽  
Claire Briet ◽  
Linda Löfbom ◽  
...  

2018 ◽  
Vol 128 (8) ◽  
pp. 3460-3474 ◽  
Author(s):  
Lorraine Yeo ◽  
Alyssa Woodwyk ◽  
Sanjana Sood ◽  
Anna Lorenc ◽  
Martin Eichmann ◽  
...  

2017 ◽  
Vol 10 (3) ◽  
pp. 897-909 ◽  
Author(s):  
Jonathan Kapke ◽  
Zachary Shaheen ◽  
Deepak Kilari ◽  
Paul Knudson ◽  
Stuart Wong

With the introduction of immune checkpoint inhibitors into clinical practice, various autoimmune toxicities have been described. Antibodies targeting the receptor:ligand pairing of programmed death receptor-1 (PD-1) and its cognate ligand programmed death-ligand 1 (PD-L1) in rare reports have been associated with autoimmune diabetes mellitus. We report 2 cases of rapid-onset, insulin-dependent, type 1 diabetes mellitus in the setting of administration of nivolumab, a fully human monoclonal antibody to PD-1, and atezolizumab, a humanized monoclonal antibody to PD-L1. This appears to be the first report of autoimmune diabetes mellitus associated with atezolizumab. In addition, we provide a brief review of similar cases reported in the literature and a discussion of potential mechanisms for this phenomenon and propose a diagnostic and treatment algorithm.


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