Biraro Irene Andia, Egesa Moses, Kimuda Simon, Smith Steven G, Toulza Frederic, Levin Jonathan, Joloba Moses, Katamba Achilles, Cose Stephen, Dockrell Hazel M, Elliott Alison M
Department of Internal Medicine, College of Health Sciences, Makerere University, P.O Box 7072, Kampala, Uganda.
Department of Immunology and Infection, London School of Hygiene &Tropical Medicine, London, UK.
BMC Infect Dis. 2015 Oct 22;15:438. doi: 10.1186/s12879-015-1201-8.
With the renewed emphasis to implement isoniazid preventive therapy (IPT) in Sub-Saharan Africa, we investigated the effect of IPT on immunological profiles among household contacts with latent tuberculosis.
Household contacts of confirmed tuberculosis patients were tested for latent tuberculosis using the QuantiFERON®-TB Gold In-Tube (QFN) assay and tuberculin skin test (TST). HIV negative contacts aged above 5 years, positive to both QFN and TST, were randomly assigned to IPT and monthly visits or monthly visits only. QFN culture supernatants from enrolment and six months' follow-up were analysed for M.tb-specific Th1, Th2, Th17, and regulatory cytokines by Luminex assay, and for M.tb-specific IgG antibody concentrations by ELISA. Effects of IPT were assessed as the net cytokine and antibody production at the end of six months.
Sixteen percent of contacts investigated (47/291) were randomised to IPT (n = 24) or no IPT (n = 23). After adjusting for baseline cytokine or antibody responses, and for presence of a BCG scar, IPT (compared to no IPT) resulted in a relative decline in M.tb-specific production of IFN gamma (adjusted mean difference at the end of six months (bootstrap 95% confidence interval (CI), p-value) -1488.6 pg/ml ((-2682.5, -294.8), p = 0.01), and IL- 2 (-213.1 pg/ml (-419.2, -7.0), p = 0.04). A similar decline was found in anti-CFP-10 antibody levels (adjusted geometric mean ratio (bootstrap 95% CI), p-value) 0.58 ((0.35, 0.98), p = 0.04). We found no effect on M.tb-specific Th2 or regulatory or Th17 cytokine responses, or on antibody concentrations to PPD and ESAT-6.
IPT led to a decrease in Th1 cytokine production, and also in the anti CFP-10 antibody concentration. This could be secondary to a reduction in mycobacterial burden or as a possible direct effect of isoniazid induced T cell apoptosis, and may have implications for protective immunity following IPT in tuberculosis-endemic countries.
ISRCTN registry, ISRCTN15705625. Registered on 30(th) September 2015.
随着在撒哈拉以南非洲地区重新强调实施异烟肼预防性治疗(IPT),我们调查了IPT对潜伏性结核家庭接触者免疫谱的影响。
使用全血γ干扰素释放试验(QFN)和结核菌素皮肤试验(TST)对确诊结核病患者的家庭接触者进行潜伏性结核检测。年龄在5岁以上、QFN和TST均呈阳性的HIV阴性接触者被随机分配接受IPT并每月随访或仅每月随访。通过Luminex检测法分析入组时和随访6个月时的QFN培养上清液中结核分枝杆菌特异性Th1、Th2、Th17和调节性细胞因子,并通过酶联免疫吸附测定法(ELISA)检测结核分枝杆菌特异性IgG抗体浓度。将IPT的效果评估为6个月末细胞因子和抗体的净产生量。
16%的受调查接触者(47/291)被随机分配接受IPT(n = 24)或不接受IPT(n = 23)。在调整基线细胞因子或抗体反应以及卡介苗瘢痕的存在情况后,与不接受IPT相比,IPT导致结核分枝杆菌特异性γ干扰素产生量相对下降(6个月末调整后平均差异(自抽样95%置信区间(CI),p值)-1488.6 pg/ml((-2682.5,-294.8),p = 0.01),以及白细胞介素-2(-213.1 pg/ml(-419.2,-7.0),p = 0.04)。抗CFP-(10)抗体水平也有类似下降(调整后几何平均比率(自抽样95%CI),p值)0.58((0.35,0.98),p = 0.04)。我们发现对结核分枝杆菌特异性Th2或调节性或Th17细胞因子反应,或对PPD和ESAT-6抗体浓度没有影响。
IPT导致Th1细胞因子产生量减少,以及抗CFP-10抗体浓度降低。这可能继发于分枝杆菌负荷的降低,或者是异烟肼诱导的T细胞凋亡的可能直接作用,并且可能对结核病流行国家IPT后的保护性免疫有影响。
ISRCTN注册库,ISRCTN15705625。于2015年9月30日注册。