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Systematic scoping review shows declining filarial infection prevalence in Latin America from 1946 to 2025Filaria Rates Drop After Mass Drug Campaigns

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Key Takeaway
Note varying diagnostic methods and focal transmission patterns limit direct prevalence comparisons across Latin American settings.

This systematic scoping review synthesizes evidence on lymphatic filariasis, onchocerciasis, and mansonellosis across Latin American populations from 1946 to 2025. The scope includes adults in endemic communities and children in transmission assessment surveys, evaluating mass drug administration (MDA) against pre-MDA baselines or different diagnostic methods.

Key findings illustrate substantial reductions in infection markers. In the Dominican Republic's La Ciénaga focus, circulating filarial antigen (CFA) positivity declined from 10.7% in 2002 to 0% in 2014. Similarly, Onchocerca volvulus skin microfilarial positivity in Guatemala's San Vicente Pacaya focus was 31% in 1976–1977, while OV16 IgG4 seropositivity in Guatemala's Huehuetenango reached 0% in children in 2007–2008. In Ecuador's Esmeraldas focus, vector infectivity (O-150 PCR) was 0% by 2008, and OV16 IgG4 seropositivity was 0% in children and adolescents in 2001–2008.

The review also reports on Mansonella ozzardi, with positivity at ~40% by whole-blood loop-mediated isothermal amplification (LAMP) and 12.7% by blood smear microscopy in Colombia's Amazonas Department in 2021–2023. In the Brazilian Amazon, positivity was 6.3% in Tefé Riverine communities and 13.6% overall in Tefé municipality surveys in 2012, compared to 43.4% in another Amazonian cohort in 2009–2010.

Authors note significant limitations, including the use of different diagnostic methods such as microscopy, antigen tests, serology, and molecular assays that vary in sensitivity and specificity. Sampling differences between adults and children, combined with highly focal transmission, mean prevalence can vary substantially even between nearby communities. Safety data and adverse events were not reported.

For years, entire communities in Latin America lived with a silent threat — tiny worms spread by biting insects, slowly damaging the body, sometimes leading to severe swelling or blindness. These are filarial infections, and they’ve affected millions across tropical regions. But now, in places once hit hard, children are growing up free of these parasites for the first time in generations.

These diseases — lymphatic filariasis (often called elephantiasis), onchocerciasis (river blindness), and mansonellosis — are caused by thread-like worms passed through mosquito or blackfly bites. They don’t spread person to person, but in areas where the bugs thrive, infection rates can soar. For decades, treatment was limited and diagnosis tricky. Now, mass drug campaigns are changing the picture — but not everywhere equally.

The Big Drop in River Blindness

In parts of Guatemala and Ecuador, river blindness once gripped entire villages. In one region, early surveys found 83% of people infected. But after years of annual treatment with ivermectin, something remarkable happened. By 2008, no children tested positive for the parasite. The transmission chain was broken. In 2009, Ecuador officially stopped mass treatment — a rare win against a neglected disease.

The same pattern emerged with lymphatic filariasis. In the Dominican Republic, over 10% of children tested positive for active infection in 2002. Just over a decade later, after three rounds of mass drugs, that number dropped to zero in young children — a sign that new infections had stopped. Haiti has seen similar progress, with less than 0.2% of children now testing positive in most areas.

Why One Disease Still Spreads

But the story isn’t the same everywhere. Mansonellosis, caused by a different worm and spread by tiny biting midges, remains common — especially in the Amazon. In parts of Brazil and Colombia, up to 43% of people tested positive in some groups. In one Colombian study, a more sensitive test found mansonellosis in nearly 40% of people — four times higher than older methods showed.

This gap matters. It means past surveys likely missed many infections. And because mass drug campaigns haven’t targeted mansonellosis as aggressively, the parasite keeps spreading.

Think of the parasite like a factory inside the body — quietly producing offspring that circulate in the blood. The drugs used — ivermectin, albendazole, diethylcarbamazine — don’t always kill the adult worms fast, but they shut down the factory. They clear the bloodstream of tiny larvae, so mosquitoes can’t pick them up and spread them further. Over time, with enough people treated, the chain breaks.

It’s not a vaccine. It’s not a one-time cure. But when entire communities take the drugs together, year after year, the odds shift. Fewer bites lead to infection. Fewer kids grow up at risk.

The Hidden Problem of Testing

Here’s the catch. Different diseases need different tests — and not all are equally accurate. Some check for antibodies, which can linger long after infection. Others look for antigens or DNA, which signal active disease. In one study, a new test found mansonellosis in 40% of people, while the old blood smear found only 13%. That means past efforts may have underestimated the problem.

Also, transmission is highly local. One village might be clear. The next, just miles away, could still be hot with infection. That makes it hard to declare any area fully safe without careful, repeated testing.

This doesn't mean this treatment is available yet.

Experts say the success against lymphatic filariasis and onchocerciasis proves mass drug campaigns can work — even in remote areas. But mansonellosis has been left behind, partly because it causes milder symptoms and gets less attention. Still, it can lead to joint pain, rashes, and eye issues. And with better tests now available, health officials may need to rethink how and where they look.

So what does this mean for people living in at-risk areas? If you’re in a region that’s had years of mass treatment for river blindness or elephantiasis, the risk to children today is far lower than it once was. But in Amazonian communities, especially in Colombia and Brazil, mansonellosis remains a quiet concern — and one that may need more focus.

There are limits. Most data come from small surveys, not nationwide tracking. Some areas haven’t been tested in years. And while drugs are safe for most, they aren’t given to everyone — like pregnant women or very ill patients — so coverage is never 100%.

The road ahead depends on better tools. Faster, cheaper tests could help find hidden outbreaks. And if new drug regimens can clear adult worms more effectively, treatment could end sooner. For now, the progress is real — but uneven. In some places, the end of filariasis is in sight. In others, the fight is just becoming visible.

7. ENDING

Health programs in Latin America now face a choice: expand current campaigns to cover mansonellosis or risk leaving entire communities behind. Research is ongoing, but without broader testing and targeted treatment, the gains made against other filarial diseases may not extend to all.

Study Details

Study typeCohort
EvidenceLevel 3
PublishedApr 2026
View Original Abstract ↓
Filarial infections—lymphatic filariasis, onchocerciasis, and mansonellosis—persist as neglected tropical diseases in Latin America despite control efforts. Comparing filarial trends over time is challenging because studies use different diagnostic methods such as microscopy, antigen tests, serology, and molecular assays that vary in sensitivity, specificity, and whether they detect active infection or past exposure, while also sampling different populations such as adults in endemic communities versus children in transmission assessment surveys. Transmission is also highly focal, so prevalence can vary substantially even between nearby communities. We searched MEDLINE, Embase, CENTRAL, LILACS, Web of Science, SciELO, and Global Health (1946–2025) to summarize reported epidemiology and burden of filarial infections in Latin America before and after mass drug administration (MDA) scale-up. For lymphatic filariasis, the Dominican Republic’s La Ciénaga focus (Santo Domingo) declined from 10.7% circulating filarial antigen (CFA) positivity in 2002 to 0% CFA-positive children (aged 6–7 years) in a 2014 transmission assessment survey (TAS) using the immunochromatographic test after three MDA rounds (2004–2006). In Haiti, Nippes Department surveys detected 1.5% CFA positivity in 2019, while pooled TAS results across 54 implementation units during 2017–2022 found 0.19% CFA positivity among children aged 6–7 years. For onchocerciasis, Guatemala’s San Vicente Pacaya focus reported 31% Onchocerca volvulus skin microfilarial positivity by skin-snip microscopy in 1976–1977, whereas Huehuetenango reported 0% OV16 IgG4 seropositivity in children in 2007–2008. In Ecuador’s Esmeraldas focus (Cayapas River area), early surveys documented 83% infection by skin-snip microscopy. In comparison, post-MDA monitoring showed 0% vector infectivity (O-150 PCR) by 2008 and 0% OV16 IgG4 seropositivity in children and adolescents (2001–2008), supporting MDA cessation in 2009. For Mansonellosis, prevalence in the Brazilian Amazon ranged from 6.3% in Tefé Riverine communities to 13.6% overall in Tefé municipality surveys (both in 2012; thick blood smear microscopy), and reached 43.4% in another Amazonian cohort (2009–2010; blood microfilariae detection by microscopy). In Colombia’s Amazonas Department (Leticia/Puerto Nariño), whole-blood loop-mediated isothermal amplification (LAMP) detected ~40% Mansonella ozzardi positivity in 2021–2023, compared with 12.7% by blood smear microscopy in the same study, illustrating diagnostic sensitivity differences. The reviewed data show clear reductions in lymphatic filariasis and onchocerciasis after MDA scale-up, whereas mansonellosis remains common in several Amazonian regions. Reported prevalence varies across studies due to differences in diagnostic approaches, surveyed populations, and localized transmission patterns.
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