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通过静脉注射致葡萄膜炎肽对实验性自身免疫性葡萄膜视网膜炎进行免疫调节。

Immunomodulation of experimental autoimmune uveoretinitis by intravenous injection of uveitogenic peptides.

作者信息

Sasamoto Y, Kawano Y I, Bouligny R, Wiggert B, Chader G J, Gery I

机构信息

Laboratory of Immunology, National Eye Institute, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

Invest Ophthalmol Vis Sci. 1992 Aug;33(9):2641-9.

PMID:1639611
Abstract

Intravenous (IV) injection of antigenic proteins induces specific unresponsiveness, as shown by the diminished response to a challenge with these proteins in complete Freund's adjuvant. This study examined the effect of IV treatment with uveitogenic peptides on the development of experimental autoimmune uveoretinitis (EAU). The peptides used were derived from the sequence of bovine interphotoreceptor retinoid-binding protein (IRBP) and included R16 (sequence, 1177-1191), which is immunodominant and highly uveitogenic, and R4 (sequence, 1158-1180), which is nondominant and weakly uveitogenic. The efficacy of this treatment was found to depend on both the dose used for the IV injection and that used for the challenge. Thus, EAU induced by R16 at a dose of 0.2 nmol/rat was inhibited completely in all rats treated with the peptide at doses of 400 or 133 nmol and partially by the low dose of 5 nmol/rat. However, the EAU induced by a R16 challenge of 40 nmol/rat was inhibited only partially by the high treatment dose of 400 nmol/rat. The IV treatment was found to be effective in inhibiting the EAU induced by peptide R4. A large dose of R4 was needed to induce EAU (40 nmol/rat), and the disease was inhibited completely in all rats treated IV with this peptide at doses of 800, 400, or 133 nmol. In most animals injected with the 44-nmol dose, also, inhibition was complete. These data show that there is a correlation between the doses needed for achieving inhibition and those used for the challenge. The ratios between these doses in all experiments were found within the range 1-20.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

静脉注射抗原性蛋白质可诱导特异性无反应性,这表现为在用这些蛋白质与完全弗氏佐剂进行激发时反应减弱。本研究检测了用葡萄膜炎原性肽进行静脉治疗对实验性自身免疫性葡萄膜视网膜炎(EAU)发展的影响。所用的肽来源于牛视网膜色素上皮细胞间维生素A结合蛋白(IRBP)的序列,包括免疫显性且高度致葡萄膜炎的R16(序列为1177 - 1191)和非显性且弱致葡萄膜炎的R4(序列为1158 - 1180)。发现这种治疗的效果取决于静脉注射所用的剂量以及激发所用的剂量。因此,以0.2 nmol/大鼠的剂量由R16诱导的EAU在所有用400或133 nmol剂量的该肽治疗的大鼠中被完全抑制,而在5 nmol/大鼠的低剂量时被部分抑制。然而,由40 nmol/大鼠的R16激发诱导的EAU仅被400 nmol/大鼠的高治疗剂量部分抑制。发现静脉治疗在抑制由肽R4诱导的EAU方面是有效的。需要大剂量的R4才能诱导EAU(40 nmol/大鼠),并且在用800、400或133 nmol该肽进行静脉治疗的所有大鼠中,该疾病被完全抑制。在大多数注射44 - nmol剂量的动物中,抑制也是完全的。这些数据表明,实现抑制所需的剂量与激发所用的剂量之间存在相关性。在所有实验中,这些剂量之间的比率在1 - 20的范围内。(摘要截短于250字)

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