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‘Funding for TB is in crisis,’ says John Green, author of Everything is Tuberculosis

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‘Funding for TB is in crisis,’ says John Green, author of Everything is Tuberculosis


John Green, author of bestselling books including The Fault In Our Stars, is a passionate campaigner for eradicating tuberculosis. In his new book, Everything is Tuberculosis, he writes about the history of the disease, the role of the U.S., and why he decided to do something about it. An edited excerpt from an interview:

A young tuberculosis patient receives medicines from a nurse at a TB hospital in Guwahati.
| Photo Credit:
AP

Your book is part poetic, part philosophical, capturing the story of a disease panning three centuries. What motivated you to write it?

About 1.25 million people died from TB in 2023. It’s overwhelming, and we don’t know how to process these kinds of numbers. I wanted to write about one person and his personal experience with tuberculosis as a way of humanising the disease. I met Henry at a tuberculosis hospital in Sierra Leone in 2019 and he looked pretty healthy, but his TB wasn’t responding well enough to antibiotics. I was in Sierra Leone to learn about maternal health, but when I came home from that trip, I learned that TB is still our deadliest infectious disease.

Patients undergoing treatment for tuberculosis at the Government Hospital of Thoracic Medicine at Tambaram Sanatorium, Chennai.
| Photo Credit:
G. Krishnaswamy

One in four TB patients who dies belongs to India. You are a strong advocate for availability of drugs. For drug-resistant TB, bedaquiline is now open to be manufactured by generic companies. How do we ensure access on the ground?

The TB response in India has gotten much better over the last 10 years due to people like Shreya Tripathi who sued her government in order to get access to the newest and best antibiotic, bedaquiline. Unfortunately, by the time Shreya won the court case and got access to bedaquiline, it was too late for her. I also tell the story of the young survivors of TB who worked with the Indian court system to establish that the bedaquiline patent should not be extended forever. India is the pharmacy of the world and that decision has made it possible for Indian manufacturers to develop bedaquiline that cost 60% less. Hopefully, that will mean fewer deaths from tuberculosis, but unfortunately, with the U.S. stepping back so much, funding to fight tuberculosis is in a real crisis now and it’s not clear who is going to step up. Countries like India have to step up into the vacuum that the U.S. has created. Many people who need bedaquiline still aren’t getting it due to complexities of distributing the medicine, especially to rural communities, and updating treatment guidelines. 

A tuberculosis patient receives medicines at a clinic in New Delhi.
| Photo Credit:
AP

Actions of the U.S. government are being felt in developing countries, including India. How do you see such decisions impacting the goal of eliminating TB?

We know that diabetes, for instance, is a huge risk factor for TB, so is HIV. Tuberculosis is the leading cause of death from AIDS and so all of this is interconnected. TB anywhere is a threat to people everywhere there is. That’s why it’s devastating to see the U.S. government walk back on its long-term commitments to health funding. Look at the progress India has made in the last 30 years on child mortality. That’s one of the greatest successes in human history and to see us taking steps backwards is absolutely devastating.

A nurse prepares to give an injection to a tuberculosis patient at the Lal Bahadur Shastri Government Hospital, in Varanasi.
| Photo Credit:
AP

You have been advocating for eradicating TB before U.S. Congress.

The U.S. should care about TB for the same reason that all rich countries should care about it, which is that we became rich largely through extractive colonialism. That has resulted in a wildly unjust and unfair global social order, where some people have access to the newest medications and treatments and other people don’t. That’s a failure of a human-built system. We should also care about tuberculosis because there are 10,000 cases of tuberculosis every year in the U.S. We have a TB outbreak right now in Kansas. This is a prime example of what happens when we don’t do a good job of distributing global resources we have to address healthcare crises. I see this as a product of history. I see the current global TB crisis as a product of the long history of distributing resources unfairly and acting as if some lives matter more than others.

Have you won the cost battle yet with your advocacy? There is major struggle in sourcing a drug of importance, delamanid, that Japan-based Otsuka pharma manufactures, due to high costs ($800-$2400 for 6 to 18 months).

We’ve won the cost battle with bedaquiline but not the distribution battle. We have not won the cost battle with delamanid and that is essential to the future of fighting tuberculosis, because for fighting drug-resistant tuberculosis, delamanid is a very important drug. In countries like India, we need far more delamanid available so that we don’t have stock outs of that critically important drug, and cost is a major barrier there.

You write that in the 19th century being inflicted with TB (known as consumption back then) was fashionable.

In the early 19th century, it was widely believed that only white people could get TB. It was seen as a very ennobling disease that made you beautiful, gave you very pale skin, red cheeks from the fever and wide eyes. All of these became beauty standards in Europe and the U.S. And it was also seen as making you super intelligent, sensitive and a wonderful poet. Charles Dickens called consumption the disease that wealth never warded off, a disease that anyone could get, no matter how rich you were. In fact, the richest person in the 19th century, Jay Gould, died of tuberculosis in his forties. It was imagined as a very different disease from the way it is imagined now, as a disease of poverty. 

In the book you write about your struggle with a highly resistant strain of infection which you treated with antibiotics.

It’s important that we invest a lot right now in finding TB cases and in treatment because of the risk of antimicrobial resistance. We are seeing TB that is resistant to more and more bacteria and we need to develop new tools and new classes of antibiotics as also do a good job of distributing current tools and making sure that people are getting timely treatment. My own experience with microbial resistance was a cellulitis infection behind my left eye, between the tissue of my brain and eye that became inflamed. My eye hurt, I went to the doctor. And everybody panicked because it’s pretty close to your brain. The infection wasn’t responding to the first or second line of antibiotics, and so I was hospitalised for a week. It was a really scary experience and it gave me a lot of time to sit, think, look at the ceiling and wonder if I was going to die as a result of this infection. But it was also a reminder that antimicrobial resistance is a threat to all of us.

An article in ‘NYT’ describes you as somebody who wants to eliminate TB, which is an entirely curable disease. As a young adult writer of influence, perhaps you’re on the right track. But you mention in the book that it is very tough to entirely eliminate TB. India has set an ambitious goal to eliminate TB by 2025. Do you think it’s hard to do that?

It would require a lot of resources to eliminate tuberculosis worldwide. But it’s a great investment because every time we end a chain of transmission, we never have to worry about it, because this is a curable disease. In the U.S., hundred years ago, we had almost as many hospital beds for TB patients as we had for all other health care conditions combined. And now we spend very little money on TB because we’ve mostly eliminated it. I believe that will be the case in India, in Sierra Leone, in South Africa. Or in the Philippines or Indonesia. But it won’t be the case until we engage in active case finding, which means sending an army of people out to find TB. Not waiting until people are so sick that they come into a clinic or hospital. It means getting treatment to every single one of those people and it means offering preventive care to their close contacts, their family members. If we did that, we could eliminate tuberculosis. It would require a big investment, but we know that it would pay off in a big way because we know that for every dollar we invest in tuberculosis research and response, we get $40 of economic benefit in return.

Can you elaborate on your advocacy with diagnostic company Danaher to reduce TB test prices?

Danaher manufactures a molecular test called GeneXpert, which can tell whether someone has TB within two hours, whether they’re resistant to one of the first line drugs, and which antibiotics is this person most likely to respond to. Unfortunately, the tests are expensive, and out of reach for low-income countries. We are still diagnosing a lot of tuberculosis through the way we used to in 1880s (by the method of X-rays and sputum microscopy.) I was a part of pressuring Danaher to lower the price of its standard TB test cartridge to produce it at cost instead of making a profit from it, since they make plenty of profit from other tests and in charging rich countries for tests. Eventually, Danaher agreed to cut the price of their test but there’s still a long way to go. But that progress is real and worth celebrating. The cost of test cartridge was $10 and now it’s $7.97.

What is your parting shot to readers when it comes to tackling TB because this is clearly going to be a long fight?

The first battle will be to get USAID and as much funding as possible back in play so that we can have at least some response to TB coming from the U.S. government. I’m also looking at prices for diagnostics and the drugs that are still too expensive, like delamanid.

Everything is Tuberculosis; John Green, Penguin Random House, ₹999.

porechamaitri.m@thehindu.co.in



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Surveillance, R&D innovation and communication are key levers for India to lead the fight against AMR

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India, with its high population density, prevalence of infectious diseases, and over-the-counter availability of antibiotics, has a long and winding road to travel in order to counter AMR. Photograph used for representational purposes only
| Photo Credit: istock.com/Dr_Microbe

Antimicrobial resistance (AMR), often labelled as a silent pandemic, is one of the most pressing global health challenges of our time. As pathogens evolve to withstand the drugs currently available to counter them, our ability to treat infections is rapidly eroding. A recent study funded by Wellcome and the United Kingdom Department of Health and Social Care’s Fleming Fund, estimates that bacterial AMR alone will cause 39 million (3.9 crore) deaths between 2025 and 2050, which translates to three deaths every minute – a shockingly stark statistic. AMR also threatens to undo decades of progress made against infectious diseases such as tuberculosis, typhoid and pneumococcal pneumonia, among others, with new multidrug resistant strains now in circulation.

In 2016, in response to the continually escalating global threat of AMR, the United Nations General Assembly (UNGA) convened its first High-Level Meeting (HLM) to address the root causes of AMR, develop national action plans, regulate antimicrobials, and promote awareness and best practices. With this mandate, many countries prepared their national action plans. India launched its plan in 2017, a six-pronged approach including improving awareness, reducing infections, optimising antimicrobial use, strengthening surveillance, increasing investment, and enhancing India’s leadership in AMR.

Last year, the UNGA reconvened for a second high-level meeting to review global progress on AMR. Its outcome was a strong political commitment by the 193 member countries to identify gaps, invest in sustainable solutions, improve R&D, strengthen surveillance, and ensure constant monitoring in the lead-up to the next review in 2029.

The path to combating AMR in India

India, with its high population density, prevalence of infectious diseases, and over-the-counter availability of antibiotics, has a long and winding road to travel in order to counter AMR. It is meeting the challenge head-on. India has not only expanded and built on its genomic surveillance capabilities to stay ahead of AMR, but government bodies such as the Indian Council of Medical Research (ICMR), the National Centre for Disease Control (NCDC) and the Indian Council of Agricultural Research (ICAR) have also established surveillance networks that focus on priority pathogen groups and communicate critical data to policymakers and researchers. However, while genomic sequencing can help track how pathogens evolve and acquire resistance, it still doesn’t have direct utility in helping clinicians make difficult, and urgent, lifesaving decisions.

India’s genomic capabilities can be most effectively leveraged in two key ways. First, public health experts should use genomic data to anticipate microbial evolutionary trajectories and emerging AMR trends. This can inform the most appropriate choice of antibiotics when patients are treated empirically (which is mostly the case). Second, diagnostic companies should use large-scale population genomics to build precision tools that could be made available at, or near the point-of-care. For example, genomic studies on Salmonella enterica serovar Typhi (the bacterium causing typhoid fever) reveal how the H58 lineage has acquired multidrug resistance over time. Researchers identified single nucleotide polymorphisms (SNPs) from whole-genome sequencing data, which are now being used to create targeted molecular diagnostics. This enables faster and more cost-effective detection of drug-resistant strains, instead of sequencing each circulating strain.

At the Christian Medical College, Vellore (CMC), the country’s reference AMR institution, researchers are sequencing representative strains to generate important epidemiological data and trends. They are also using genomic markers for rapid and robust diagnosis, supporting the national AMR efforts under the mentorship of ICMR.

The urgent need for new drugs

In addition to enhanced surveillance and smart diagnostics, we urgently need new drugs. Developing new antimicrobials is scientifically complex, financially risky, and often commercially unattractive. India’s robust biotech ecosystem, high burden of endemic infectious diseases, and proven capacity for affordable manufacturing create the ideal environment for innovation. When these strengths are combined, they will not only accelerate India’s fight against AMR but also improve global access, especially for low- and middle-income countries (LMICs).

Recent breakthroughs from India, such as the introduction of novel antibiotics like cefepime-enmetazobactam, cefepime-zidebactam, nafithromycin, and levodifloxacin, mark a significant global advancement in the fight against multidrug-resistant pathogens, particularly the WHO’s critical priority threats. These drugs offer new therapeutic options that can reduce reliance on carbapenems and last-resort agents like colistin. At a time when the world is looking at a fast-drying antibiotic pipeline, this progress offers a glimmer of hope. Such leadership in developing new antibiotics underscores India’s growing scientific and regulatory capabilities, paving the way for increased international collaboration and faster global approvals.

A communication strategy

Given the magnitude of the AMR crisis, genomic surveillance and integrated public health systems can only work efficiently if they are supported by a carefully designed communication strategy to improve awareness. In India, where antibiotics can often be bought over the counter without a prescription, innovative and human-centered advocacy should be prioritised more than it currently is. This includes antimicrobial stewardship among healthcare professionals, including both physicians, pharmacists and other unorthodox or informal practitioners that form an important pillar of frontline healthcare delivery. Moreover, it should be reiterated that vaccination is not just important in preventing viral diseases that do not require antimicrobial treatment or multidrug resistant diseases, but also in reducing antimicrobial usage.

To communicate the gravity of the situation effectively, innovations that can simplify data and generate actionable evidence will play a central role. One such example is AMRSense, an award-winning collaboration between IIIT-Delhi, CHRI-PATH, and 1mg.com, which is using AI to collect data across the clinical, animal, and environmental axes in a true One Health approach and using predictive modeling to guide targeted interventions.

The challenge of tackling AMR is immense, and we are at an inflection point. Acting alone or in an uncoordinated and siloed fashion will not produce the desired results. India has the tools, the talent, and the urgency to lead the world in curbing antimicrobial resistance. But all scientific efforts need to be unified and communicated to the general public and experts alike, in ways that resonate with them. Only then will we be on our way to winning the fight against AMR.

(Dr. Ankur Mutreja is a genome scientist and microbiologist, and the Director, Strategy, Partnerships and Communications at PATH. amutreja@path.org Dr. Tikesh Bisen is a Public Health Specialist – Surveillance at PATH. tbisen@path.org Dr. Balaji Veeraraghavan is a Professor at the Christian Medical College & Hospital, Vellore. His research focus is on vaccine-preventable invasive bacterial diseases and Antimicrobial Resistance in clinically relevant pathogens. vbalaji@cmcvellore.ac.in)



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Looking back to the strength of a people’s movement against filariasis

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The World Health Organization has sought to eliminate filariasis, globally, by 2030, a decade later than its original target of 2020. While India’s target year is now 2027, this deadline has been arrived at after several revisions: the National Health Policy had originally set the goalpost for 2015. Filariasis, clearly, has been difficult disease to eradicate.

While pioneering experiments by vector specialists over the years have helped India reduce its disease burden, consistent efforts are needed to eliminate the disease, reports have acknowledged. 

“Filariasis is the common term for a group of diseases caused by parasitic nematodes belonging to the superfamily Filarioidea. Adult worms of these parasites live in the lymphatic system, cutaneous tissues or body cavity of the humans and are transmitted through vectors”, explains a documents from the National Centre for Vector Borne Diseases Control.

Filariasis caused by nematodes that live in the human lymph system is called Lymphatic Filariasis (LF). The burden of lymphatic filariasis is massive in India, with as many as 670 million persons at risk for the disease, according to a report published in the Indian Journal of Medical Research in 2022. 

While the disease has been around for decades in India, there still exist many misconceptions about it, says S. Sabesan, former director of the Indian Council of Medical Research — Vector Control Research Centre, Puducherry.

General filariasis care focuses on preventing mosquito bites, treating infections with medication, and managing the symptoms and potential complications of the disease. 
PHOTO: THE HINDU ARCHIVES

Kerala’s story with filariasis

Kerala  was instrumental in spotlighting filariasis in India. In 1984-85, a group of filariasis affected persons in Alappuzha formed an association, and its president contested the general election that year, aiming to attract the attention of politicians and bureaucrats. It bore fruit. A Member of Parliament from Kerala S. Krishna Kumar, became the deputy minister in the Union Health Ministry. He called for action against filariasis in Kerala, which set the ball rolling, recalls Dr. Sabesan. 

Kerala’s culture of associations helped to further the project of eliminating filariasis, he says. All associations were amassed under the umbrella of the Filariasis control movement or ‘Filco‘ movement. The project targeted removing floating vegetation where mosquitoes that cause the disease breed. The mosquitoes lay eggs on leaves and the larvae absorb oxygen from the air sacs in the roots of the plants. Understanding the breeding pattern of the mosquitoes helped remove the floating vegetation, which was then placed as manure in coconut groves.

To control mosquitoes the State Health Department also targeted Kerala’s large resource of ponds and water bodies to develop aquaculture, using fish from dams. The fish would feed on the larvae, curtailing mosquito breeding.

Interdepartmental support

Support also came from Kerala’s Agriculture Department which saw the potential of improving livelihoods in rural areas. Shramdhan workers cleaned temple tanks, canals and water bodies, and NABARD pitched in with financial support to remove the plants, and establish aquaculture.

In two years, inland fisheries had been developed. To add value to the removed water vegetation, hemp was cultivated. This improved the quality of fertilisers that coconut groves received. Ultimately, the Health Department roped in the Education Department to raise an army of schoolchildren who could spread awareness to help improve adherence to treatment of the disease. 

The Health Department also used the knowledge of how village residents checked the feet of eligible young women to check if they harboured the disease before offering a marriage proposal. The Department made a young woman with lymphatic oedema, in whose family many women had been rejected owing to the disease, their mascot. The young woman recovered from filariasis after treatment and this boosted people’s confidence. Her story was made into a short film, Yudham (war) and exhibited, giving further fillip to treating the disease. Alongside, the Department trained Filco workers to detect the disease and bring in patients for treatment.

Free clinics were opened to offer treatment. The next step was checking for hidden disease, which involved mass drug administration. Soon, the number of cases fell drastically indicating that the disease was in the elimination stage.

The Kerala Health Department’s approach included collaborating with the Agriculture Department to develop aquaculture, engaging schoolchildren for awareness, and using a recovered patient as a mascot. Mass drug administration and training workers to detect and treat the disease led to a significant reduction in cases, pushing filariasis towards elimination. Picture shows an awareness campaign on filariasis held in Tamil Nadu (Photo taken on August 21, 1987)
PHOTO: THE HINDU ARCHIVES

A win, and a mass strategy

The success of the experiment was shared at the WHO’s meeting in 1996 in Kuala Lampur and the World Health Assembly decided on a strategy of administering a single dose of diethylcarbamazine citrate (DEC).

In India, the annual single dose mass therapy was introduced in 2002, but the nation-wide the scheme did not help in eliminating the disease, for want of follow-up care.

In 2006, the Union Health Ministry introduced the drug Albandazole that can have an effect on adult worms of the parasite. But there was a lack of compliance, even though the drugs were distributed. The Health Ministry found that despite distributing the drug there, was no reduction in the number of cases.

Meanwhile in Kerala another development took place.

The salt story

Through a project, salt-infused with a low dose of the drug DEC was introduced in Kerala. This project was launched with the support of the salt corporation in Thoothukudi in Tamil Nadu. Within a year, the number of filariasis cases fell significantly. The project’s success was expanded in Tamil Nadu’s Kanyakumari district in 2003. 

By 2020, the Indian Council of Medical Research launched DEC salt in Andaman and Nicobar and successfully eliminated another variety of filariasis. This salt therapy could be used as an adjunct therapy across the country Dr. Sabesan has said in the white paper he has published on the subject: Not only is it odourless, but it also doesn’t change the colour of food and is safe for pregnant women and children as well. 

For the success to be sustained it is imperative that we achieve the target of elimination, he says. “Tamil Nadu is doing well. But filariasis is found in Karnataka, Andhra Pradesh, Bihar and Uttar Pradesh as well. There are areas where filariasis is a challenge. If uncontrolled, filariasis will be reintroduced, as the vector is already present in the atmosphere. The low density carriers will build up gradually. So it is necessary to continue surveillance even after elimination is declared. Vector entomologists must focus on the mosquitoes and the vector,” he emphasises.



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Over 9,400 new HIV cases detected in Telangana in 2024

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Telangana State AIDS Control Society (TSACS) presented data on the number of HIV cases detected in Telangana in 2024. The image is used for representative purposes only.
| Photo Credit: RAMAKRISHNA G

As many as 9,415 people in Telangana tested positive for HIV in 2024, according to data presented by the Telangana State AIDS Control Society (TSACS). The figures emerged during a high-level review meeting chaired by Minister for Health C. Damodar Raja Narasimha on Monday.

A total of 19.02 lakh individuals were tested for HIV in the State during the year. Officials informed the Minister that approximately 1.24 lakh people living with HIV were currently receiving free treatment through the network of Antiretroviral Therapy (ART) centres across Telangana.

TSACS officials said that more than 5,000 HIV patients were concentrated in 13 districts, while another 13 districts had between 2,000 to 5,000 patients. The Minister instructed health officials to scale up testing in all districts, especially targeting high-risk groups, and to intensify awareness programmes to curb the spread of the virus.

He stressed the need to regularly assess the performance of NGOs working in collaboration with TSACS. “The State government is committed to the goal of eliminating HIV AIDS by 2030. All our efforts should be directed toward this objective,” he said.



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