Busch M P, Switzer W M, Murphy E L, Thomson R, Heneine W
Blood Centers of the Pacific, CA, USA.
Transfusion. 2000 Apr;40(4):443-9. doi: 10.1046/j.1537-2995.2000.40040443.x.
Recent identification of divergent simian or primate T-lymphotropic viruses (STLVs; PTLVs) in bonobos (formerly called pygmy chimpanzees; Pan paniscus; viruses: STLVpan-p and STLVpp1664) and a baboon (Papio hamadryas; viruses: STLVph969 or PTLV-L) have raised the possibility of human infection with these viruses. Divergent PTLV-infected primate sera show p24 bands on HTLV-I Western blots (WBs). It was investigated whether infection by divergent PTLV-like viruses could explain a subset of United States blood donors who reacted on HTLV-I EIAs and had indeterminate HTLV-I WBs with p24 bands.
Epidemiologic characteristics of 1889 donors with HTLV-I-indeterminate WBs were compared to those of donors with confirmed retrovirus infections (393 with HIV, 201 with HTLV-I, 513 with HTLV-II) and 1.6 million donors with nonreactive screening tests. To directly probe for infection with divergent PTLVs, 2 HTLV-I-indeterminate donors born in Africa and 269 representative non-African-born donors with p24 bands on HTLV-I WBs (previously shown to be negative for HTLV-I and -II DNA by PCR) were selected for PTLV PCR analysis. DNA from peripheral blood MNC samples was tested for a proviral tax sequence by PCR using generic primers that amplify HTLV-I, HTLV-II, and the divergent PTLVs. Amplified tax sequences were detected by Southern blot hybridization to a (32)P-labeled generic PTLV probe. PCR-positive samples could then be typed by hybridization with virus-specific internal probes that differentiate HTLV-I, HTLV-II, PTLV-L, and STLVpan-p.
In the epidemiologic analysis, HTLV-indeterminate status was independently associated with age of at least 25 years (OR = 2.19; 95% CI, 1.93-2.49), black (OR = 3.27; 95% CI, 2.90-3.67) or Hispanic (OR = 1.82; 95% CI, 1.52-2.16) race or ethnicity, and donation at one blood center (Baltimore) (OR = 1. 30; 95% CI, 1.11-1.53). None of the 271 HTLV-I WB-indeterminate samples tested positive by generic PTLV PCR analysis.
Although the epidemiologic data suggest the possibility of undiagnosed HTLV-I, HTLV-II, or a cross-reactive virus such as PTLV among older, black, and Hispanic blood donors, the PCR data do not support the presence of divergent PTLV infection among US blood donors with HTLV-I-indeterminate results.
最近在倭黑猩猩(以前称为矮黑猩猩;倭黑猩猩属;病毒:STLVpan-p和STLVpp1664)和一只狒狒(阿拉伯狒狒;病毒:STLVph969或PTLV-L)中发现了不同的猿猴或灵长类嗜T淋巴细胞病毒(STLVs;PTLVs),这增加了人类感染这些病毒的可能性。感染不同PTLV的灵长类动物血清在HTLV-I免疫印迹法(WBs)上显示p24条带。研究了感染不同PTLV样病毒是否可以解释在美国HTLV-I酶免疫测定(EIAs)反应阳性且HTLV-I WBs结果不确定且有p24条带的献血者中的一部分情况。
将1889名HTLV-I WB结果不确定的献血者的流行病学特征与确诊的逆转录病毒感染献血者(393名HIV感染者、201名HTLV-I感染者、513名HTLV-II感染者)以及160万名筛查试验无反应的献血者进行比较。为了直接检测是否感染不同的PTLV,选择了2名出生在非洲的HTLV-I结果不确定的献血者和269名在HTLV-I WBs上有p24条带(先前通过PCR显示HTLV-I和-II DNA为阴性)的有代表性的非非洲出生的献血者进行PTLV PCR分析。使用扩增HTLV-I、HTLV-II和不同PTLV的通用引物,通过PCR检测外周血单个核细胞(MNC)样本中的DNA是否存在前病毒tax序列。通过与(32)P标记的通用PTLV探针进行Southern印迹杂交检测扩增的tax序列。然后,PCR阳性样本可以通过与区分HTLV-I、HTLV-II、PTLV-L和STLVpan-p的病毒特异性内部探针杂交进行分型。
在流行病学分析中,HTLV结果不确定状态与至少25岁的年龄(比值比[OR]=2.19;95%置信区间[CI],1.93-2.49)、黑人(OR=3.27;95%CI,2.90-3.67)或西班牙裔(OR=1.82;95%CI,1.52-2.16)种族或民族以及在一个血液中心(巴尔的摩)献血(OR=1.30;95%CI,1.11-1.53)独立相关。271份HTLV-I WB结果不确定的样本中,没有一份通过通用PTLV PCR分析检测为阳性。
尽管流行病学数据表明在年龄较大、黑人和西班牙裔献血者中可能存在未诊断的HTLV-I、HTLV-II或一种交叉反应病毒如PTLV,但PCR数据不支持在美国HTLV-I结果不确定的献血者中存在不同PTLV感染。