Production of IL-8 and IL-4 by positively and negatively selected CD4+ and CD8+ human T cells following a four-step cell separation method including magnetic cell sorting ( MACS)

1996 ◽  
Vol 189 (1) ◽  
pp. 107-115 ◽  
Author(s):  
Luminita A. Stanciu ◽  
Janis Shute ◽  
Stephen T. Holgate ◽  
Ratko Djukanović
Nanoscale ◽  
2017 ◽  
Vol 9 (36) ◽  
pp. 13592-13599 ◽  
Author(s):  
Qian Zhang ◽  
Ting Yin ◽  
Rongrong Xu ◽  
Wenjun Gao ◽  
Hui Zhao ◽  
...  

A self-designed high-throughput system has been developed for large-scale immuno-magnetic cell sorting of different T cells.


2021 ◽  
Vol 7 (5) ◽  
pp. 58
Author(s):  
Tianya Liang ◽  
Jianxing Li ◽  
Xiao Liu ◽  
Zhuang Ma ◽  
Xiaojin Su ◽  
...  

Immunomagnetic beads (IMBs) for cell sorting are universally used in medical and biological fields. At present, the IMBs on the market are ferrite coated with a silicon shell. Based on a new type of magnetic material, the graphene coated iron nitride magnetic particle (G@FeN-MP), which we previously reported, we prepared a novel IMB, a graphene oxide coated iron nitride immune magnetic bead (GO@FeN-IMBs), and explored its feasibility for cell sorting. First, the surface of the G@FeN-MP was oxidized to produce oxygen-containing groups as carboxyl, etc. by the optimized Hummers’ method, followed by a homogenization procedure to make the particles uniform in size and dispersive. The carboxy groups generated were then condensed and coupled with anti-CD3 antibodies by the carbodiimide method to produce an anti-CD3-GO@FeN-IMB after the coupling efficacy was proved by bovine serum albumin (BSA) and labeled antibodies. Finally, the anti-CD3-GO@FeN-IMBs were incubated with a cell mixture containing human T cells. With the aid of a magnetic stand, the T cells were successfully isolated from the cell mixture. The isolated T cells turned out to be intact and could proliferate with the activation of the IMBs. The results show that the G@FeN-MP can be modified for IMB preparation, and the anti-CD3-GO@FeN-IMBs we prepared can potentially separate T cells.


Blood ◽  
2011 ◽  
Vol 118 (19) ◽  
pp. 5174-5177 ◽  
Author(s):  
Christian Hofmann ◽  
Sandra Höfflin ◽  
Angela Hückelhoven ◽  
Silke Bergmann ◽  
Ellen Harrer ◽  
...  

AbstractAdoptive TCR transfer against rapidly mutating targets, such as HIV-1 or cancer, must counteract corresponding immune escape. Hence, we generated T cells expressing two additional receptors (TETARs) specific for HIV-1 by TCR mRNA electroporation. An HLA-A2–restricted gag-specific TCR and an HLA-B13–restricted nef-specific TCR were chosen. When both TCRs were transfected simultaneously, strong competitive effects occurred that were overcome by replacing the human constant domains of one TCR with murine counterparts and adapting the amounts of TCR-RNA used for transfection. The resulting TETAR responded to both epitopes with cytokine secretion and cytotoxic function. Cell sorting revealed that one individual cell indeed recognized both epitopes. The T cells diminished their reactivity to each epitope after stimulation but sequentially killed targets that presented the gag epitope and then targets that presented the nef epitope, or vice versa. Taken together, TETARs represent a sophisticated tool to study TCR functionality and might be a useful strategy in immunotherapy.


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