Results 261 to 270 of about 790,770 (284)
Some of the next articles are maybe not open access.

Nanobodies targeting the interaction interface of programmed death receptor 1 (PD-1)/PD-1 ligand 1 (PD-1/PD-L1)

Preparative Biochemistry & Biotechnology, 2019
Targeting the interaction interface is an effective strategy to obtain programmed death receptor 1 (PD-1)/PD-1 ligand 1 (PD-L1) nanobody blockers. To validate this strategy, the interaction interface between PD-1 and the PD-L1 extracellular domain were analyzed using Cn3D 4.1. The peptide PD-1125-136 located at the interface of PD-1 was selected as the
Biyan, Wen   +8 more
openaire   +2 more sources

Molecular Imaging of PD-1 Unveils Unknown Characteristics of PD-1 Itself by Visualizing “PD-1 Microclusters”

Programmed cell death-1 (PD-1) is one of the most famous coinhibitory receptors that are expressed on effector T cells to regulate their function. The PD-1 ligands, PD-L1 and PD-L2, are expressed by various cells throughout the body at steady state and their expression was further regulated within different pathological conditions such as tumor-bearing
Wataru, Nishi   +11 more
openaire   +2 more sources

Glucocorticoids and PD-1

Science Signaling, 2018
Signaling by the glucocorticoid receptor in NK cells induces expression of the checkpoint inhibitor PD-1 to prevent immunopathology.
openaire   +1 more source

Targeting PD-1

Science Signaling, 2018
Loss of an E3 ubiquitin ligase that targets PD-1 for degradation leads to inefficient antitumor responses by T cells.
openaire   +1 more source

Pretreatment CD8+PD-1+ to CD4+PD-1+ ratio is associated with the prognosis of advanced melanoma patients treated with PD-1 inhibitors

Melanoma Research
The aim of this study was to determine whether the pretreatment CD8+PD-1+ to CD4+PD-1+ (PERLS) ratio is an independent risk prognostic factor of advanced melanoma patients. We retrospectively analyzed the efficacy and flow cytometry data from advanced melanoma patients who received PD-1 inhibitor as monotherapy between January 1, 2018 and January 26 ...
Yao, Gao   +9 more
openaire   +2 more sources

FBXO38 Drives PD-1 to Destruction

Trends in Immunology, 2019
Aberrant expression of T cell-resident programmed cell death protein-1 (PD-1) is known to promote tumor progression. A recent study (Nature 2018;564:130-135) has now identified the E3 ubiquitin ligase FBXO38 as a crucial regulator of PD-1 protein turnover in T cells, providing a novel mechanism for potential use in cancer immunotherapy.
Taryn M, Serman, Michaela U, Gack
openaire   +2 more sources

Reactions of iodobenzene on Pd(1 1 1) and Pd(1 1 0)

Applied Surface Science, 2003
Abstract We have investigated the formation and reaction of phenyl fragments on Pd(1 1 1) and Pd(1 1 0), using synchrotron radiation-based photoelectron spectroscopy. The phenyl fragments are formed by carboniodine bond scission of iodobenzene, taking place already at 80 K. Pd(1 1 0) is seen to be more reactive than Pd(1 1 1) in this reaction.
H. von Schenck   +4 more
openaire   +1 more source

Tug of war with anti–PD-1

Science, 2017
Cancer Antibodies against immune checkpoint proteins such as programmed cell death 1 (PD-1) are gaining increasing prominence in cancer treatment, but these promising therapeutics do not always work. To be effective in preventing T cells from becoming exhausted, antibodies against PD-1 must remain bound to the T cells. Arlauckas et al.
openaire   +2 more sources

PD-1/PD-L1 in Disease

Immunotherapy, 2017
Expression of PD-1 on T/B cells regulates peripheral tolerance and autoimmunity. Binding of PD-1 to its ligand, PD-L1, leads to protection against self-reactivity. In contrary, tumor cells have evolved immune escape mechanisms whereby overexpression of PD-L1 induces anergy and/or apoptosis of PD-1 positive T cells by interfering with T cell receptor ...
Kuol, Nyanbol   +3 more
openaire   +3 more sources

Role of PD-1 in Immunity and Diseases

2017
Immunity developed to defend our bodies from foreign particles, including bacteria and viruses. Although effector cells responsible for acquired immunity, mainly T cells, and B cells, are able to distinguish self from non-self, they sometimes attack the body's tissues because of imperfect central tolerance.
Kenji, Chamoto   +2 more
openaire   +2 more sources

Home - About - Disclaimer - Privacy