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几内亚比绍否认批准在新生儿中开展有争议的疫苗试验

Guinea-Bissau denies it has approved controversial vaccine trial in newborns

The Guardian 原文署名:Melody Schreiber原文发布:2026年10月14日 21:16 · 北京时间

以下为原文逐段中文翻译,保留图表与说明。AI 翻译并经 AI 对照复核,仍可能存在错误;核对数据和引用时请同时查看原文。译文发布:2026年10月17日 06:30(北京时间)。

这个非洲国家的卫生部长周二说,几内亚比绍没有批准一项由美国政府和私人伙伴资助、在新生儿中开展的有争议的乙型肝炎研究。

这项研究不会调查疫苗的安全性及有效性,而是追踪总体死亡率或神经发育状况等“非特异性”健康结果。它得到美国卫生与公众服务部(HHS)部长、长期反疫苗活动人士小罗伯特·F·肯尼迪的力挺。

丹麦一个研究伦理委员会的成员被告知,几内亚比绍官员已批准该研究的更新版设计,这影响了部分委员会成员上周投票赞成推进该试验。

但卫生部从未同意或授权这项试验,金欣·南托特在一场新闻发布会上用葡萄牙语说。他在会上把这项研究称为“检测”。

“卫生部没有按照当前流传的出版物中所呈现的条件授权这些检测,”这位卫生部长说。他说,几内亚比绍官员看到媒体报道称该国批准了这项研究时感到“惊讶”。

“任何涉及人类、尤其是儿童的科学科研活动,都必须严格遵守适用的国家法律、国际伦理原则以及有资质机构的评估和审批机制,”南托特说。

他是在几内亚比绍与班丁健康项目、当地伦理委员会、国家公共卫生研究所(Inasa)和扩大疫苗接种计划(PAV)召开紧急会议后说这番话的。

班丁健康项目由丹麦研究人员彼得·奥比和克里斯蒂娜·斯塔贝尔·本主持,他们数十年的研究在过去一年中受到质疑。

丹麦研究员夏洛特·斯特伦说,他们几乎所有论文中提出的主张都“极具误导性”。她参与合著的研究表明,奥比、斯塔贝尔·本及其合著者在 25 项研究中有 24 项没有得出显著发现,并且他们选择不发表可能不支持其观点的研究。

“当研究人员这样行事、抛弃恰当的方法学严谨性时,他们实际上是在自行决定结果,而这并非科学,”斯特伦说,称其“有问题、可疑[且]不道德”。

她补充说:“我认为有严重的理由感到担忧。”

肯尼迪一再称赞他们的工作,他说这些工作表明,接种疫苗后,“可能会出现大规模伤害和灾难性伤害,而它们就隐藏在大庭广众之下”。

截至发稿时,奥比、斯塔贝尔·本和弗雷德里克·沙尔茨-布赫霍尔策尚未回应《卫报》的提问,即为何丹麦伦理委员会成员被告知该试验已获当地政府批准,以及为何不能在丹麦进行。

在丹麦,乙肝阴性父母所生的婴儿不接种该疫苗,病毒检测广泛且发病率低,健全的医疗体系能够追踪健康结果并提供及时、全面的医疗服务——这使其成为开展此类研究的理想地点。

埃默里大学研究员 BK·蒂坦吉说,“这项试验竟然被提出,本身就不道德”,因为安全有效的疫苗已经问世数十年。

蒂坦吉说,看到几内亚比绍抵制这项试验“令人欣慰”,并补充说:“像这样的研究需要最高级别的伦理审查。你将要在一个资源有限的国家,对最脆弱的人群——新生儿——开展研究。”

蒂坦吉说,当她最近为在喀麦隆开展一项合作研究申请批准时,她必须在申请中附上大量文件——而那只是一项调查,并非针对人类受试者的医学研究。“我不能到埃默里大学的(机构审查委员会)就说:‘我得到了喀麦隆的许可。’我必须提供文件。”

她说,研究人员应当公开这些文件以及一份说明研究将如何开展的更新版方案。

专家们谴责这项在非洲进行的实验“极不道德且残忍”、“带有新殖民主义色彩”且“具有破坏性”。

研究员、非营利组织“为科学挺身而出”(Stand Up for Science)创始人兼首席执行官科莱特·德拉瓦拉说:“几内亚比绍政府挺身对抗美国和丹麦对其儿童的利用,绝非等闲之举。我们绝对必须尊重他们作为一个国家的主权。”

德拉瓦拉指出,通过联合国儿童基金会和全球疫苗免疫联盟(Gavi)购买足够的疫苗,为几内亚比绍每年所有新生儿接种,大约需要 13,200 美元。

她补充说,所有相关方应共同努力,确保几内亚比绍的每个婴儿都接种出生剂量的乙肝疫苗。“这不是一潭浑水:我们可以利用黑人婴儿来推进伪科学,也可以用一剂 20 美分的疫苗来拯救儿童的生命。”

目前尚不清楚美国是否计划推进这项研究,即便有报道显示美国疾病控制与预防中心(CDC)今年再次拨出 160 万美元用于资助该试验,并将由潘兴广场基金会和蓝铃基金会的私人资金予以匹配。

HHS 在给路透社的一份声明中说:“该研究尚未获得批准。”该机构尚未回应《卫报》关于这项试验的提问。

在该试验的批准被快速推进后,丹麦委员会至少有四名成员辞职。委员会规则不得不做出修改,因为随机对照试验原本不在其职权范围内。当委员会成员要求提供关于几内亚比绍批准情况的更多信息时,并未提供进一步细节。

该研究将在几内亚比绍招募 14,000 名新生儿,其中一半在出生时接种疫苗,另一半在出生后头六周内不接种该疫苗。乙型肝炎在该国广泛流行,儿童感染可能造成严重的终身影响。

几内亚比绍在去年 11 月发生政变后目前由过渡军政府执政,该国于今年 1 月请求非洲疾病控制与预防中心(Africa CDC)派专家团队协助评估这项研究。南托特当时说,在此期间,该研究已被“取消或暂停”。

几内亚比绍的其他官员也抵制这项研究。外交部长若昂·贝尔纳多·维埃拉在 2 月说:“这不会发生,就这样。”

世界卫生组织(WHO)已提出支持在几内亚比绍为所有新生儿推广出生时接种乙肝疫苗。“世卫组织随时准备支持几内亚比绍考虑其前进方向,并加快引入出生剂量和加强落实,”该组织在 2 月一份抵制该试验的声明中说。

展开英文原文 · 与中文逐段对应

Guinea-Bissau denies it has approved controversial vaccine trial in newborns

Guinea-Bissau has not approved the controversial hepatitis B study in newborns that would be funded by the US government and private partners, the African country’s minister of health said on Tuesday.

The study, which would not investigate the safety or effectiveness of vaccines but would instead track “nonspecific” health outcomes like overall mortality or neurodevelopmental conditions, has been championed by Robert F Kennedy Jr , secretary of the US Department of Health and Human Services (HHS) and a longtime anti-vaccine activist.

Members of a Danish research ethics committee were informed that officials in Guinea-Bissau had approved an updated design of the study, which influenced some committee members’ votes to proceed with the trial last week.

But the health ministry never agreed to or authorized the trial, said Quinhin Nantote in Portuguese at a press briefing , where he referred to the study as “tests”.

“The ministry did not authorize the tests under the terms presented in the publications currently in circulation,” the health minister said. He said officials in Guinea-Bissau were “surprised” to see media reports that the country had given approval to the study.

“Any scientific research initiative involving human beings, particularly children, ‌must ⁠strictly comply with applicable national legislation, international ethical principles, competent evaluation and approval mechanisms,” Nantote said.

He spoke after convening an emergency meeting in Guinea-Bissau with the Bandim Health Project, the local ethics committee, the National Institute of Public Health (Inasa) and the Expanded Vaccination Program (PAV).

The Bandim Health Project is run by the Danish researchers Peter Aaby and Christine Stabell Benn, whose decades of research have been called into question in the past year.

The claims made in nearly all of their papers are “highly misleading”, said Charlotte Strøm, a Danish researcher who has co-authored research showing that Aaby, Stabell Benn, and their co-authors had no significant findings in 24 out of 25 studies and that they’ve chosen not to publish research that may not support their viewpoints.

“When researchers operate like this and abandon proper methodological rigor, they literally decide on the results themselves, and that is not science,” Strøm said, calling it “problematic, questionable [and] unethical”.

She added: “I believe there is serious cause for concern.”

Kennedy has repeatedly praised their work, which he says shows that after vaccination, “you can have mass injuries, and catastrophic injuries, and they’re hiding in plain sight”.

Aaby, Stabell Benn and Frederik Schaltz-Buchholzer did not respond by press time to the Guardian’s questions about why the Danish ethics committee members were told the trial had been approved by local authorities and why it could not be held in Denmark.

In Denmark, infants born to hepatitis B-negative parents do not receive the shot, there is widespread testing for and low incidence of the virus, and the robust healthcare system can track health outcomes and provide timely and comprehensive medical care – making it an ideal location for such a study.

“It’s completely unethical that this trial is even proposed,” because a safe and effective vaccine has been available for decades, said BK Titanji, a researcher at Emory University.

It’s “reassuring” to see Guinea-Bissau pushing back on the trial, Titanji said, adding: “A study like this one needs the highest level of ethical scrutiny. You are going to be conducting a study on the most vulnerable population, which is newborn babies, in a country that is resource-constrained.”

When Titanji recently applied for approval of a collaborative study in Cameroon, she had to include extensive documentation in her application – and it was a survey, not medical research on human subjects, she said. “I can’t come to Emory’s [institutional review board] and just be like: ‘I got permission from Cameroon.’ I have to provide the document.”

The researchers should release these documents and an updated protocol showing how the study would be conducted, she said.

Experts have decried the African experiment as “ horribly unethical and cruel ”, “ neocolonialist ” and “ damaging ”.

“For the government of Guinea-Bissau to stand up against the United States and Denmark exploiting its children is no small statement,” said Colette Delawalla, a researcher and founder and CEO of the non-profit Stand Up for Science. “We absolutely must respect their sovereignty as a nation.”

It would cost approximately $13,200 to buy enough vaccines through Unicef and Gavi, the Vaccine Alliance, to immunize all newborns in Guinea-Bissau each year, Delawalla pointed out.

Everyone involved should work together to ensure that every baby in Guinea-Bissau receives the birth dose of the hepatitis B vaccination, she added. “This is not muddy water: we can use Black babies to further pseudoscience or we can save children’s lives with a 20-cent shot.”

It is unclear whether the US plans to move forward with the study, even after reporting indicated that the US Centers for Disease Control and Prevention (CDC) has again set aside $1.6m for funding for the trial this year, to be matched by private funding from the Pershing Square Foundation and the Bluebell Foundation.

“The ​study has ⁠not been approved,” the HHS told Reuters in a statement. The agency has not responded to the Guardian’s questions about the trial.

At least four members of the Danish committee resigned after approval for the trial was fast-tracked. The rules of the committee had to be changed because randomized controlled trials were outside of its purview. When committee members requested more information about the Guinea-Bissau approval, no further details were provided.

The study would enroll 14,000 newborns in Guinea-Bissau, half of whom would be vaccinated at birth and half of whom would be denied the immunization for the first six weeks of life. Hepatitis B is widespread in the country, and infection in children can have serious lifelong effects.

Guinea-Bissau, which currently has a transitional military government following a coup in November, requested in January a team of experts from the Africa Centres for Disease Control and Prevention (Africa CDC) to help evaluate the study. In the meantime, Nantote said at the time, it was “ canceled or suspended ”.

Other officials in Guinea-Bissau also pushed back on the research. “It’s not going to happen, period,” the foreign minister, João Bernardo Vieira, said in February.

The World Health Organization (WHO) has offered support in rolling out the hepatitis B vaccine at birth to all newborns in Guinea-Bissau. “WHO stands ready to support Guinea‑Bissau as it considers its way forward and in accelerating the introduction of the birth dose and strengthening implementation,” the organization said in a February statement pushing back on the trial.

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据《卫报》报道,几内亚比绍卫生部长周二表示,该国并未批准一项在新生儿中开展的、由美国政府及私人伙伴资助的争议性乙型肝炎研究。报道称,该研究不会考察疫苗的安全性或有效性,而是追踪整体死亡率、神经发育状况等「非特异性」健康结果,并得到美国卫生与公众服务部部长、长期反对疫苗的罗伯特·F·肯尼迪二世的支持。一个丹麦研究伦理委员会成员曾获悉几内亚比绍官员已批准该研究的更新设计,这影响了部分成员上周投票同意推进试验。但卫生部长昆欣·南托特在记者会上用葡萄牙语表示,卫生部从未同意或授权该试验。

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