在机体免疫系统中，B淋巴细胞和T淋巴细胞协同起来识别抗原。
The biological immune system employs B-Cell and T-Cell in detecting antigen.
细胞只能识别抗原提呈细胞表面特定的抗原肽MHC分子复合物，这就是T细胞抗原识别的MHC限制。
T cell can only recognize specific antigenic peptide-MHC complex on antigen-presenting cell. This is MHC restriction in antigen recognition of t cell.
确定T细胞所识别抗原分子上的短肽序列对T细胞表位进行定位，对于研究特异性免疫应答有着重要意义。
It is very crucial to identify antigen peptide recognized by t cell to study adaptive immune response and immune regulation.
细胞在成熟过程中通过T细胞表面受体基因重排，从而具有特异性识别抗原的能力，在这一过程中的任何失调都会导致疾病。
T cell receptor (TCR)gene rearrangement is an important event in T cell ontogeny that enables T cells to specifically recognise antigens, and any dysregulation in this process may result in diseases.
抗原被巨噬细胞加工表示该抗原将被淋巴细胞识别。
Antigen processing by macrophages precedes recognition of an antigen by lymphocytes.
如果某一个助细胞识别出一个抗原，该助细胞就会被活化。
If a helper cell recognises an antigen, it becomes activated.
细胞到达靶器官、识别移植的异体抗原，启动一系列变化。
The T cell arrives at the target organ, the recognition transplant foreign body antigen, starts a series of changes.
该抗血清不但能识别来源于大肠杆菌的抗原，还能检测真核细胞内转染后表达的IRF-7。
The antisera can recognize not only recombinant IRF-7 expressed in E. coli, but also transfected IRF-7 in mammalian cells.
这项新的研究显示，哪怕是只有一种自身抗原没有被识别为“自身”成分，这个识别缺欠就有可能会导致视网膜发生严重的自身免疫性疾病。
The new research showed that if just one of the body's antigens is not recognized as "self," this single failure can lead to a severe autoimmune disease in the retina.
当T细胞识别肿瘤上的抗原时，这些细胞能直接与肿瘤细胞相互作用。
When the T cells recognized the antigen, they interacted directly with the tumor cells.
数字序列抗原内部存在许多语义特征，针对抗原进行语义识别可以提高系统检测的准确性。
There are many semantics in digit sequence antigen space. It can improve the accuracy of system detection to recognize upon the semantics of antigens.
母体对胎儿抗原的错误识别或与父方的HLA相容性增高，都会抑制其抗-HLA抗体的产生。
Inadequate recognition of fetal antigens or increased sharing of human leukocyte antigens with the father may inhibit the production of anti-HLA antibodies.
肥大细胞除具有识别、吞噬并杀灭病原微生物的功能外，尚能加工、递呈抗原和调节免疫反应。
Mast cells not only have the ability to recognize and phagocytize pathogens, then kill them, but they can also present antigens and regulate immunity response.
CD 1蛋白与MHC分子的结构非常相似，然而二者识别结合的抗原物质却在生化性质及物理结构上有本质的区别。
Although the structure of CD1 molecules is very similar to that of MHC molecules, there are essential differences in the biochemical character and physical structure of antigens recognized by them.
淋巴细胞识别由主要组织相容性复合物（MHC）I或II类分子递呈的抗原肽片段。
T lymphocytes recognize antigenic peptide fragments presented by major histocompatibility complex(MHC) class I or class II molecules.
MG 7抗体是一种单克隆抗体，它所识别的MG 7抗原是一种胃癌相关抗原。
The antibody MG7 is a monoclonal antibody and the antigen MG7 recognized by which is one of tumor - associated antigens.
细胞和T细胞可对对抗原刺激识别和反应。
Both B and t cells function in the recognition of, and response to, antigenic stimulation.
激光扫描共聚焦显微镜观察显示，单抗6A8识别的分化抗原见于3D5细胞浆和胞膜。
The examination upon a lazer scan confocal microscope revealed the expression of the differentiation antigen recognized by McAb 6A8 both on the membrane and in the cytoplasm of 3D5 cell.
在此基础上，模拟生物体的抗原识别、免疫应答等实际免疫行为，提出一种新的人工免疫算法。
Then simulating the antigen identify of organism, immune response and other actual immune behavior, a new artificial immune algorithm is put forward.
提出了一种免疫聚类算法，该算法主要包括抗体产生、抗原识别和抗体优化等过程。
In this paper, an immune clustering algorithm is presented, which includes antibody production, antigen recognition, and antibody optimization.
然而，在诊断方法上还是取得了一些显著的进展，如培养方法的改进、菌株的快速识别和新型抗原分析用于检测真菌血症。
However, some notable improvements have been made in diagnostics with improved culturing methods, rapid species identification, and detection of fungemia with newer antigen assays.
因此，树突状细胞(DC细胞)递呈肿瘤抗原给共培养的CIK细胞，希望可以增强CIK细胞识别肿瘤的能力以及提高其肿瘤杀伤活性。
Hence, dendritic cells (DC) were cultured and engineered to present tumor antigens to CIK cells hoping that this might enhance the recognition of tumor cells and its subsequent killing.
结论细胞免疫能够获得识别组织特异性抗原抗体，能够为后继实验研究、诊断和治疗打下基础。
Cell immunization could be used obtaining mAbs recognizing tissue-specific antigens and which would be useful for the future research, diagnosis and therapy at proteinome period.
叠加实验表明，5A5、5C12和6F5三株单抗抗原识别位点均不相同。
The results of superposable test suggest that 5A5, 5C12 and 6F5 were against different antigen epitope.
以前有没有方法来识别的抗原没有事先知道触发其生产的抗体（有针对性的免疫分子型）。
There has previously been no way to identify an antibody (a type of targeted immune molecule) without first knowing the antigen that triggers its production.
所述抗原和含有上述组分的T辅助淋巴细胞识别部位二者通过疏水相互作用或共价键附着到一个类脂上而与脂质体缔合。
Both the antigen and the T-helper lymphocyte recognition site containing constituent may be associated with the liposome by using hydrophobic interactions or by covalent attachment to a lipid.
结论具有活性的多肽分子与HLA-A2限制性TIL识别的人黑色素瘤特异性抗原肽有关。
Conclusion These results showed that peptides derived from three active fractions were related to human melanoma-specific pep- tide antigens recognized by HLA-A2-restricted TIL.
基因组学的到来使高通量筛选肿瘤特异性转录和突变成为可能，随即能够识别异常的共用及单一肿瘤相关抗原。
The advent of genomics allows a high-throughput screening for tumor-specific transcripts and mutations, with that identifying novel Shared and unique TAA.
该抗体识别的抗原CPS1可表达于肺癌细胞的细胞膜，可能是一个肺癌靶向治疗的新靶位。
CPS1, the antigen of 1e2, locates on the membrane of lung cancer cells and it may become a novel molecule target for lung caner therapy.
该抗体识别的抗原CPS1可表达于肺癌细胞的细胞膜，可能是一个肺癌靶向治疗的新靶位。
CPS1, the antigen of 1e2, locates on the membrane of lung cancer cells and it may become a novel molecule target for lung caner therapy.
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