轉移免疫 的英文怎麼說

中文拼音 [zhuǎnmiǎn]
轉移免疫 英文
transfer immunity
  • : 轉構詞成分。
  • : Ⅰ動詞1. (移動) move; remove; shift 2. (改變; 變動) change; alter Ⅱ名詞(姓氏) a surname
  • : Ⅰ動詞1 (去掉;除掉) dismiss; relieve; remove 2 (避免) avoid; escape; avert 3 (免去) excuse s...
  • : 名詞(瘟疫) epidemic disease; pestilence
  • 轉移 : 1 (改換位置) shift; transfer; divert 2 (改變) change; transform 3 [醫學] (擴散) metastasis;...
  1. Section two the evaluation of biocompatibility of the acellular dermal matrix by the method of cell culture. the new born rat ' s epdermic cells were cultured with the acellular dermal matrix together as experiment group, while the epdermic cell were cultured simply as control. 24 hours later, under the invert microscope, the epidermic cells anchored well and transparent flat cells were observed in both groups. 7 days later, both cultured cells were taked out and fixed in 95 % ethanol, stained with hematoxylin and were observed under light microscope. many cleaved cells were observed in both groups. during cell culture, no pathogenic microganism was observed. so we considered the acellular dermal matrix was aseptic and had good biocompatibility. section three subdermal implantation of the acellular dermal matrix. 24 rats were used in the experiments. a piece of acellular dermal matrix ( 1. 5 x 1. 5cm2 ) was implanted beneath the dorsum skin flaps of each rat, 1 week, 2 weeks, 3 weeks and 4 weeks after implantation, 6 pieces of acellular dermal matrix were harvested and the size of implanted acellular dermal matrix were measured, the sections were used for he staining and observed under light microscope. the result were as folio wing : 1 - 2 weeks after implantation, the acellular dermal matrix began to adhere to the tissue around and turned red gradually ; 3 - 4weeks after implantation, the acellular dermal matrix adhered closely to the tissue around and could be recognized easily, 1 - 3 weeks after implantation, the size of implanted acellular dermal matrix had no statistical difference ( p > 0. 05 ). 4 weeks after implantation implanted acellular dermal matrix contracted ( p < 0. 05 ). under light microscope, l - 2weeks after implantation, the fibroblast cells infiltrated the acellular dermal matrix and a small amount endothelial cells of vessel and lympho - histiocytic cells infiltrated the acellular dermal matrix. 3 - 4 weeks after implantation, infiltrating blood vessels were evident. so we think that the acellular dermal matrix had low immunological reactions and could induce the infiltration of fibroblast macrophage cell and the endothelial cells of vessel

    結果如下:皮下包埋卜周者,無細胞真皮基質漸與周圍組織粘附,顏色由蒼白紅;皮下包埋3周者,無細胞真皮基質與周圍組織緊密枯附,盾晰葉辯;術后卜周,包埋的基質面積變化較包埋前無統計學差異o川0引,術后4周包埋的無細胞真皮基質面積較包埋前縮小j刃刀5 ) 。光鏡下術后卜周,宿主的淋巳組織細胞、成纖維細胞浸入生長,釉附在膠原纖維上,少量血管內皮細胞浸入基質;術后34周,無細胞真皮基質內較多的血管形成,故可認為無細胞真皮基質原性低,能誘導宿主的成纖維細胞、巨噬細胞浸入生長,為一種新型的真皮替代物。第四部分無細胞真皮基質與自體斷層皮片復合棺的研究, sd大鼠10隻,在其背部卜方造成全厚皮膚缺損的創面
  2. 2. rat orthotopic liver trarlsplantation was performed in the strong rejecter combination of bn ( rtl " ) to lew ( rtl l ). this al1ogenic rejection model was stable and the survival time without immunosuppression agents was less than three weeks ( the average survival time was l 6. 6 i 2. 5 days, n = 5 )

    建立了大鼠bn ( rt1 ~ n ) lew ( rt1 ~ l )原位肝植同種異體排斥模型,該模博士學位論義基因hu la個ig誘導大鼠植肝耐受的實驗研究中文摘要型排斥反應時間較為恆定,在不應用抑制劑的情況下,生存期3周(平均生存時問人66士2
  3. Functions : this product contains “ antifungal active protein ” with optimal and strong sterilization effect, which could strengthen the immunity of body fluid, activate the macrophage, strengthen the phagocytosis ability of macrophage, strengthen the body immunity, restrain the growth, pervasion and transfer of abnormal cells, the product has strong sterilization effect and could strengthen the disease resistance ; it is remarkably effective in improving the immunity and improving the infirm constitution of pets ; the amino acid content and composition in the product are moderate and rational, with the characteristics of strong palatability, nutrition balance and immune element abundance, etc

    功能:本產品中擁有極佳強烈殺菌作用的「抗菌活性蛋白」 ,能增強體液功能,活化巨噬細胞,增強其吞噬能力,可增強機體力,抑制非正常細胞生長、擴散和,具有強烈的殺毒作用,增強抗病性;對提高寵物力,改善虛弱體質有顯著效果;其中氨基酸含量適中、組成合理,具有適口性強、營養均衡和物質豐富等特點。
  4. The protein product of meq gene was highly expressed in the nuclei of recombinant baculovirus infected sf9 cells when using an anti - meq monoclonal antibody ( mcab ) 23b46 to run the immunofluorescence assay ( fa ) ; the expression quantity and if staining patterns differed with different times post - infection ( pi ). the results of western blotting and immunoprecipitation test showed there were two specific bands around 60 kd. the results of the study demonstrated that the baculovirus / insect cell system is effective to be used to express nuclear protein of virus

    結果發現:本表達系統產生的meq蛋白可被重組痘病毒表達的meq制備的單抗23b46所識別;在感染細胞中, meq蛋白僅局限於細胞核內,而且隨著感染后( pi )時間的增加,具有從核質向核仁和核膜的趨向; w已stemblot和沉澱試驗均證實重組桿狀病毒感染細胞裂解物中出現有兩條大小約為60kd的特異帶。
  5. Activity evaluation assay proved that ultrafilter graft was better than dialysis. 6. the comparison of gpif immunobiologic activity with the similar drugs. when we compared the immunobiologic activity of gpif to thymopolypeptides solution, thymopolypeptides enteric - coated tablets and tansfer factor solution, the checking results indicated that immunobiologic activity of gpif was higher than the similar drugs, which were produced and saled in chongqing

    6 、 gpif與同類藥品生物活性比較研究我們在對比gpif與所有重慶市制藥企業生產的以及在重慶市銷售的同類藥品胸腺膚注射液、胸腺膚腸溶片(膠囊)和因子注射液生物活性時發現,採用此標準制備的gp工f生物活性高於同類產品生物活性。
  6. These shifts hae spawned noel strategies for long - term graft acceptance through reprogramming of the immune system. new paradigms proide the focus of this reiew

    這些範式換誕生了新的治療策略,通過重組機體系統實現長期的植耐受(存活) 。本綜述探討的主要焦點是新的範式。
  7. Although the development of relatively non - toxic immunosuppressive or tolerance - inducing regimens will be required to justify clinical trials using pig organs, recent advances in our understanding of the biology of xenograft rejection and zoonotic infections, and the generation of alpha1, 3 - galactosyltransferase - deficient pigs have moved this approach closer to clinical application

    盡管用豬的器官進行臨床試驗尚有賴于相對無毒的抑制劑或致耐方法的發展,但是我們在異種植排斥反應及豬源人畜共患病等方面生物學知識的進步,以及1 , 3半乳糖酶缺陷豬的產生,已經使異種植離臨床應用更近了一步。
  8. Although the deelopment of relatiely non - toxic immunosuppressie or tolerance - inducing regimens will be required to justify clinical trials using pig organs, recent adances in our understanding of the biology of xenograft rejection and zoonotic infections, and the generation of alpha1, 3 - galactosyltransferase - deficient pigs hae moed this approach closer to clinical application

    盡管用豬的器官去驗證臨床試驗需要相對無毒的抑制劑或致耐的方法,但隨著近來我們對異種植排斥生物學及動物傳染病感染的深入理解,以及1 , 3半乳糖酶缺陷豬的產生,異種植更接近臨床應用。
  9. Methods : in cultured lung explants without serum, the lipid component synthesis of pulmonary surfactant was evaluated in [ 3h ] - choline incorporation ; mrna content of phosphocholine cytidylyltransferase ( cct ) in lung explants was investigated in rt - pcr ; the changes of the ultrastructure of the at ii cells were observed with electron microscope ; the expression of nmdar1 subtype was observed in immunohistochemistry staining ; nitric oxide synthase ( nos ) activity, nitric oxide ( no ) content, superoxide dismutase ( sod ) level, malondialdehyde ( mda ) content and lactae dehydroase ( ldh ) level were determined by biochemistry methods. results : 1. influence of glutamate on synthesis of the lipid component of pulmonary surfactant ? with l - arginine, glu inhibited [ 3h ] - choline incorporation with good dose - dependence and time - dependence ; ( 2 ) mrna content of cct of the glu treatment groups was decreased ; ( 3 ) glu increases the release of ldh in cultured lung explants ; ( dwith electron microscope histochemistry, glu induced the changes of the ultrastruture of at ii iv cells

    方法:採用成年大鼠肺組織無血清培養,運用[ ~ 3h ] -膽堿摻入法測定ps主要脂質磷脂酰膽堿( pc )合成量; rt - pcr擴增檢測肺組織中pc合成限速酶磷酸膽堿二胞苷酰基酶( cct ) mrna含量;透射電子顯微鏡法觀察肺泡型上皮細胞和ps系統超微結構的變化;組織化學染色檢測glu的受體nmdar1亞單位的表達;生化測定肺組織乳酸脫氫酶( ldh )釋放量和肺組織勻漿中一氧化氮合酶( nos )活性、一氧化氮( no )生成量、超氧化物歧化酶( sod )水平以及丙二醛( mda )含量。
  10. - 1, 4 - gt seems to play a multifunctional role hi normal cell physiology and has been associated with sperm - egg binding, cell - cell recognition, cell migration on basal lamina and neurite extension, embryonic maturation, rheumatoid arthritis, and cell development. hi this paper, it is studied on expression of the - 1, 4 - gt gene

    細胞質膜上的- 1 , 4 - gt與精子的受精作用、胚胎形成、內分泌、神經元細胞的遷、癌細胞的、表皮細胞的增殖及自體性疾病等方面都有著密切的關系。
  11. Using ex vivo gene transfer technique, exogenous gene was introduced to the liver graft during cold preservation and express locally in the graft. the effect of inhibition of rejection and inducing liver graft tolerance was observed. through this study, the possibility of achieving graft tolerance by gene transfer without routine immunosuppressive drugs was explored

    我們採用adeasy腺病毒載體系統,自行構建攜帶huctla4 - ig的重組腺病毒,通過先體外后體內( exvivo )基因技術,于供肝冷保存時,將該治療基因導入大鼠植肝,使其于植肝局部表達,觀察其抑制排斥反應,誘導大鼠植肝耐受的作用。
  12. Preparation of severe acute respiratory syndrome coronavirus specific transfer factor and the study on its immunological activities

    嚴重急性呼吸綜合征冠狀病毒特異因子的制備及其活性研究
  13. Adenoviral - mediated transfer to graft of immunoregulatory genes is a novel strategy to mod [ 1latil1g in1l11une " responses

    腺病毒介導的針對植物的調節基因的,是調控反應的新策略。
  14. Robert neville : day one thousand and one. i am still unable to transfer my immunity to infected hosts

    羅伯特?奈維爾:第1001天,我仍然沒辦法把我身體里的力,給被感染的人體。
  15. Objective the aim of this article was to induce long term survival allografts by blocking cd40 - cd40l pathway with homemade anti - cd40l monoclonal antibody mr1, then purify cd4 + cd25 + regulatory t cells from recipients with long term survival allografts, and adoptively cotransfer such cells together with tcr transgenic allogenic antigen specific cd8 + t cells into immunodeffient mouse. finally study whether cd4 + cd25 + t cells can suppress allogenic antigen specific cd8 + t cell mediated rejection, thus clarified whether cd4 + cd25 + t cell mediated regulation is one of mechanisms of prolongation of allograft survival by cd40 - - cd40l pathway blockade

    植物長期存活的受體內分選出cd4 + cd25 + t細胞,與tcr基因cds + t細胞同時過繼輸注到缺陷小鼠體內,觀察co4 + co25 + t細胞對同種異體反應性cos + t細胞介導排斥反應的作用,探討在阻斷cd40se一~ cd40l共刺激途徑延長植物存活中, cd4 + cd25 +調節性丁細胞是否是抑制排斥反應的機制之一。
  16. These conventional approaches cannot be selectively targeted to the tumor cells and completely eradicate them, this may account for the development of recurrence and metastasis of gastric cancer due to the existence of residual tumor cells ; in addition, as to some kinds of conventional approaches, such as chemical therapy, their tumoricidal effects also could cause damage to some other normal tissues / cells and undermine the function of immune system in patients with gastric cancer

    目前,臨床上的?些常規方法,包括外科手術的、化學的及物理的治療手段,對絕大多數中晚期胃癌的療效均不理想。其原因在於這些常規方法對癌細胞缺乏選擇性,並不能特異性地殺傷癌細胞,勢必造成殘存癌細胞引起的腫瘤復發和。某些常規方法,如化療,在殺傷癌細胞的同時,也會造成機體正常組織的損傷並削弱機體的機能。
  17. Here magnetic resonance - trackable magnetocapsules hae been used simultaneously to immunoprotect pancreatic beta - cells and to monitor, non - inasiely in real - time, hepatic deliery and engraftment by magnetic resonance imaging ( mri )

    在這里,由磁共振跟蹤的磁性微囊已經運用於對胰島細胞進行保護,同時在磁共振成像下實時無創監測植物在肝臟運和定植。
  18. Here magnetic resonance - trackable magnetocapsules have been used simultaneously to immunoprotect pancreatic beta - cells and to monitor, non - invasively in real - time, hepatic delivery and engraftment by magnetic resonance imaging ( mri )

    在這里,由磁共振跟蹤的磁性微囊已經運用於對胰島細胞進行保護,同時在磁共振成像下實時無創監測植物在肝臟運和定植。
  19. We reviewed the advances of detective methods of new immunology and gene on gastric carcinoma metastasis, and discussed the combinative application of multi - markers detection

    綜述了有關胃癌浸潤分子和基因的研究現狀,提出了新的學診斷指標在預測腫瘤方面的應用,以及多項指標聯合檢測的可能性。
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