نتایج جستجو برای: antigen modification

تعداد نتایج: 324768  

Journal: :Cancer research 2008
Harjeet Singh Pallavi R Manuri Simon Olivares Navid Dara Margaret J Dawson Helen Huls Perry B Hackett Donald B Kohn Elizabeth J Shpall Richard E Champlin Laurence J N Cooper

Genetic modification of clinical-grade T cells is undertaken to augment function, including redirecting specificity for desired antigen. We and others have introduced a chimeric antigen receptor (CAR) to enable T cells to recognize lineage-specific tumor antigen, such as CD19, and early-phase human trials are currently assessing safety and feasibility. However, a significant barrier to next-gen...

2016
Hanren Dai Yao Wang Xuechun Lu Weidong Han

The genetic modification and characterization of T-cells with chimeric antigen receptors (CARs) allow functionally distinct T-cell subsets to recognize specific tumor cells. The incorporation of costimulatory molecules or cytokines can enable engineered T-cells to eliminate tumor cells. CARs are generated by fusing the antigen-binding region of a monoclonal antibody (mAb) or other ligand to mem...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2011
Conrad R Cruz Ulrike Gerdemann Ann M Leen Jessica A Shafer Stephanie Ku Benjamin Tzou Terzah M Horton Andrea Sheehan Amanda Copeland Anas Younes Cliona M Rooney Helen E Heslop Catherine M Bollard

PURPOSE Patients with Hodgkin lymphoma (HL) relapsing after hematopoietic stem cell transplant have limited options for long-term cure. We have shown that infused cytotoxic T cells (CTL) targeting Epstein Barr virus (EBV)-derived proteins induced complete remissions in EBV(+) HL patients. A limitation of this approach is that up to 70% of relapsed HL tumors are EBV-negative. For these patients,...

2012
Jae Hun Shin Hyung Bae Park Yu Mi Oh Dong Pyo Lim Ji Eun Lee Hae Hyun Seo Sang Jin Lee Hyeon Seok Eom In-Hoo Kim Seung Hoon Lee Kyungho Choi

Cytotoxic T lymphocyte–associated antigen 4 (CTLA4) has been known to be a strong tolerance-inducing inhibitory receptor on T-cell surface. Systemic blocking of CTLA4 function with blocking antibodies has been regarded as an attractive strategy to enhance antitumor immunity. However, this strategy accompanies systemic autoimmune side effects that are sometimesproblematic.Therefore,wedeveloped a...

2017
Marie A. Chattaway David R. Greig Amy Gentle Hassan B. Hartman Timothy J. Dallman Claire Jenkins

National surveillance of Shigella flexneri ensures the rapid detection of outbreaks to facilitate public health investigation and intervention strategies. In this study, we used whole-genome sequencing (WGS) to type S. flexneri in order to detect linked cases and support epidemiological investigations. We prospectively analyzed 330 isolates of S. flexneri received at the Gastrointestinal Bacter...

Journal: :Blood 2012
Jae Hun Shin Hyung Bae Park Yu Mi Oh Dong Pyo Lim Ji Eun Lee Hae Hyun Seo Sang Jin Lee Hyeon Seok Eom In-Hoo Kim Seung Hoon Lee Kyungho Choi

Cytotoxic T lymphocyte-associated antigen 4 (CTLA4) has been known to be a strong tolerance-inducing inhibitory receptor on T-cell surface. Systemic blocking of CTLA4 function with blocking antibodies has been regarded as an attractive strategy to enhance antitumor immunity. However, this strategy accompanies systemic autoimmune side effects that are sometimes problematic. Therefore, we develop...

2016
Ingeborg Streng-Ouwehand Nataschja I Ho Manja Litjens Hakan Kalay Martine Annemarie Boks Lenneke A M Cornelissen Satwinder Kaur Singh Eirikur Saeland Juan J Garcia-Vallejo Ferry A Ossendorp Wendy W J Unger Yvette van Kooyk

Antigen uptake by dendritic cells and intracellular routing of antigens to specific compartments is regulated by C-type lectin receptors that recognize glycan structures. We show that the modification of Ovalbumin (OVA) with the glycan-structure Lewis(X) (Le(X)) re-directs OVA to the C-type lectin receptor MGL1. Le(X)-modification of OVA favored Th1 skewing of CD4(+) T cells and enhanced cross-...

Journal: :Journal of clinical pathology 1986
P A Nuttall

Modification of the Serodia HBe haemagglutination kit produced by Fujirebio Incorporated, Tokyo, Japan, gave a rapid, economical, and easily performed test for hepatitis Be antigen (HBeAg). The use of this method to test serum samples for HBeAg is described. A modification of the kit to screen for anti-HBe is also described. The results obtained showed that this kit, when used by the method des...

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