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memory response
All the four altered proteins were responsible for bacterial stress, but cryptocyanin seemed to be a memory response protein against the challenge by a live bacterium after immunization of the live cells.
      
These assumptions are evaluated utilizing a clinically important epitope repertoire derived from two human cytomegalovirus proteins, and data on the in vitro memory response elicited by these peptides is presented.
      
parvum administered during a primary immune response has selective effects on the cytotoxic memory response.
      
CD4+ T cells are associated with antigen memory response and helper function, therefore activation of CD4+ CTL may be more beneficial with respect to long-term protective antimelanoma immunity.
      
In contrast, Flt3-ligand treatment of NXS2-bearing mice induced a protective T-cell-dependent antitumor memory response.
      
Mice possessing these activated T lymphocytes, when evaluated for their antitumor memory response, showed marginal protection against intravenous (i.v.) and subcutaneous (s.c.) tumor rechallenge.
      
E75 vaccination induced recruitment of both CD4+ and CD8+ na?ve T cells while memory response remained stable.
      
The secondary immune response was earlier and markedly stronger in non-transgenic mice compared with the transgenic mice where a less efficient memory response to gp120 was observed.
      
The IgG antibody titer showed a mean 31-fold increase (range 3-154) 4 weeks after the first vaccination and a memory response was observed after booster vaccination, i.e.
      
These results suggest that the immune response elicited by 16-mDC and 16+mDC is modified when memory or na?ve T cells are stimulated, and 16+mDC could favor a stronger and more beneficial antitumoral Th1 memory response in vivo.
      
Unlike its peptides, the GAD protein antigen did not recall a T cell memory response.
      
Rechallenge experiment showed that a persistent memory response was successfully induced by the combined therapy.
      
Single-crystal orientations of NiTi10Cu alloys were studied under incremental, cyclic compression conditions to establish the pseudoelastic and shape memory response of this class of alloys.
      
The large-deformation, self-thermal-plastic behavior of the composite material was clearly the result of a powerful shape-memory response in the NiTi composite fiber actuators.
      
Although virus administered intranasally to young calves with maternal antibodies does not evoke antibody responses, it can prime these calves for a protective memory response upon reinfection.
      
The key issues concerning memory T cells in transplantation are related to the tolerability of alloreactive memory T cells and the effects of commonly used immunosuppressive drugs on the memory response in transplant recipients.
      
Additionally, we show that memory response from distinct T cell subsets persist in the lung allograft and PBMC often long after primary infection.
      
A memory response was apparent for the second serologic response.
      
All animals were also reinoculated with the same material at 84 days to study the memory response.
      
At present we are unsure how to explain the enhanced durability of the T helper cell memory response expanded by the HEC V3.
      
 

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