Svennerholm A M, Gothefors L, Sack D A, Bardhan P K, Holmgren J
Bull World Health Organ. 1984;62(6):909-18.
A single oral or intramuscular immunization with purified cholera B subunit induced an intestinal secretory immunoglobulin A (IgA) antitoxin response in, respectively, 10 out of 11 and 9 out of 12 Bangladeshi volunteers. The IgA titre rise in intestinal lavage fluid was similar by either route of immunization, but the duration of the response was usually longer after the oral dose. A second immunization by either route, given 25 days after the first, and a third dose (oral only), given 15 months later, resulted in intestinal immune responses which did not differ in magnitude from that induced by the initial immunization but were observed significantly earlier, usually by day 3. Both the first oral and intramuscular immunizations induced significant antitoxin titre rises, mainly IgG, in the serum in most vaccinees but the magnitude of the response was considerably higher after the intramuscular dose. Significant IgA antitoxin titre rises in saliva and breast milk were seen after both oral and intramuscular immunization.
用纯化的霍乱B亚单位进行单次口服或肌内免疫,分别在11名孟加拉志愿者中的10名以及12名中的9名体内诱导出肠道分泌型免疫球蛋白A(IgA)抗毒素反应。通过任何一种免疫途径,肠道灌洗液中IgA滴度的升高情况相似,但口服免疫后反应持续时间通常更长。在首次免疫25天后通过任何一种途径进行第二次免疫,并在15个月后进行第三次剂量(仅口服)免疫,所产生的肠道免疫反应在强度上与初次免疫所诱导的反应并无差异,但出现得明显更早,通常在第3天就可观察到。在大多数接种疫苗者中,首次口服和肌内免疫均在血清中诱导出显著的抗毒素滴度升高,主要是IgG,但肌内注射剂量后的反应强度要高得多。口服和肌内免疫后,唾液和母乳中均出现了显著的IgA抗毒素滴度升高。