dc.contributor.author | Elgheriyani, Mohammed Abdulhakim | |
dc.date.accessioned | 2020-07-07T10:09:50Z | |
dc.date.available | 2020-07-07T10:09:50Z | |
dc.date.issued | 2020-03-03 | |
dc.identifier.uri | http://repository.limu.edu.ly/handle/123456789/1728 | |
dc.description | The existence of inhibitory pathways that limit T-cell response has been the target of
checkpoint inhibitors, the best example is CTLA-4 which inhibits T-cell activity by
binding to B7 and interfering with CD28-B7 costimulation and by binding to CD-80
and CD-86 (1) in addition to programmed cell death (PD-1) first discovered in mice,
carries a role in inducing "peripheral tolerance" of T cells by binding to PDL-1 in
APCs and thereby stopping an immune response(2) the mechanism of PD-1 blockade,
which is induced by IFN-y | en_US |
dc.description.abstract | Different cancers affect millions of people around the world and is considered one of
humanity's greatest challenges, traditionally cancer is tackled by therapeutic methods
such as radiation or surgery, chemotherapy as well as transplant. Activating immune
cells is a relatively old concept dating back to the early 20th century, whereby they
would be able to attack cancer cells via CD8 T cytotoxic cells but the inherent
principle of our immune system is the ability to distinguish "self" from "non-self", for
example when the T cells recognize a molecule as "non-self" for instance a cancer
cell, they attach onto the molecule initiating the immune response, in addition, there
are also accelerators and inhibitors, which provide a tight control that prevent
excessive activation and autoimmune diseases, Cytotoxic T lymphocyte associated
protein 4 (CTLA-4) is one of these brakes that can be manipulated to unleash the full
on destruction of tumour cells by CD8 cells, there is also the programmed cell death
(PD-1) molecules on T cells that interact with PD-L1 on Antigen presenting cells, by
inhibiting these brakes with blocking antibodies, reduction of cancers such as
metastatic melanoma can be achieved in addition to small cell carcinoma, renal
carcinoma and lymphoma | en_US |
dc.language.iso | en | en_US |
dc.publisher | faculty of Basic Medical Science - Libyan International Medical University | en_US |
dc.rights | Attribution 3.0 United States | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/us/ | * |
dc.title | Immune Regulation Inhibition and Its Usage and Effectiveness In Cancer Therapy | en_US |
dc.type | Other | en_US |