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Anti-PD1 Immunotherapy for Metastatic Renal Cancer Boosted Humoral Immunity in a Hemodialysis Patient

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Autore
Eleftheriadis T., Pissas G., Liakopoulos V., Stefanidis I.
Data
2021
Language
en
DOI
10.1097/CJI.0000000000000365
Soggetto
hepatitis B surface antigen
nivolumab
recombinant hepatitis B vaccine
hepatitis B antibody
hepatitis B surface antigen
hepatitis B vaccine
nivolumab
PDCD1 protein, human
programmed death 1 receptor
adult
antigen blood level
Article
cancer immunotherapy
case report
clinical article
disease predisposition
drug tolerability
electrochemiluminescence
follow up
hemodialysis patient
hepatitis B
human
humoral immunity
kidney hypoplasia
lung metastasis
lung nodule
male
memory cell
middle aged
nephrectomy
plasma cell
priority journal
renal cell carcinoma
treatment response
vaccination
hemodialysis
hepatitis B
humoral immunity
immunology
immunotherapy
kidney tumor
metabolism
procedures
Hepatitis B
Hepatitis B Antibodies
Hepatitis B Surface Antigens
Hepatitis B Vaccines
Humans
Immune Checkpoint Inhibitors
Immunity, Humoral
Immunotherapy
Kidney Neoplasms
Male
Memory B Cells
Middle Aged
Nivolumab
Programmed Cell Death 1 Receptor
Renal Dialysis
Lippincott Williams and Wilkins
Mostra tutti i dati dell'item
Abstract
Immune checkpoint inhibitors by blocking specific inhibitory pathways induce T-cell-mediated tumor lysis. However, many remain to be elucidated about their effect on human humoral immunity. We evaluated the effect of the PD1 inhibitor nivolumab on humoral immunity by following the levels of antibodies against hepatitis B surface antigen (anti-HBs) in a hemodialysis patient successfully vaccinated against hepatitis B virus 5 years ago and now starting nivolumab for renal cell carcinoma lung metastases. Anti-HBs kinetics after administration of an extra vaccine dose were also evaluated. Nivolumab increased anti-HBs and facilitated a further increase following an additional vaccine dose. The observed time frame indicates that nivolumab boosts humoral immune response by affecting long-lived plasma cells and at least memory B cells. This may protect cancer patients from pathogens encountered in the past or against which vaccination has been performed and provide information for the emerging immune checkpoint inhibitors administration concept against chronic infectious diseases. © 2021 Lippincott Williams and Wilkins. All rights reserved.
URI
http://hdl.handle.net/11615/71340
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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