# Epidemiology and Clinical Outcomes of HTLV‐1: A Comprehensive Narrative Review of Endemic and Nonendemic Regions

**Authors:** Bezhan Noori, Ramin Shahbahrami, Yousef Douzandegan, Sayed-Hamidreza Mozhgani, Mehdi Norouzi, Seyed Mohammad Jazayeri

PMC · DOI: 10.1155/cjid/8667755 · The Canadian Journal of Infectious Diseases & Medical Microbiology = Journal Canadien des Maladies Infectieuses et de la Microbiologie Médicale · 2026-02-22

## TL;DR

This paper reviews the global distribution and health impacts of HTLV-1, highlighting its severe effects in endemic regions and the need for targeted public health strategies.

## Contribution

The study provides a comprehensive narrative review of HTLV-1 epidemiology and clinical outcomes across endemic and nonendemic regions.

## Key findings

- HTLV-1 prevalence is highest in regions like Japan, Brazil, and Indigenous Australia, with significant variations within populations.
- HAM/TSP incidence is notably higher in Brazil compared to Japan, indicating regional differences in clinical outcomes.
- Effective interventions like antenatal screening in Japan have reduced transmission, but low-resource regions still face significant challenges.

## Abstract

Human T‐lymphotropic virus Type 1 (HTLV‐1) is a globally distributed, oncogenic retrovirus endemic in specific regions, including southwestern Japan, sub‐Saharan Africa, the Caribbean, parts of South America (notably Brazil), Iran, and Indigenous communities in Australia. Although most infections are asymptomatic, a minority of carriers develop severe, life‐altering conditions: adult T‐cell leukemia/lymphoma (ATL) or HTLV‐1‐associated myelopathy/tropical spastic paraparesis (HAM/TSP). This narrative review presents a comprehensive analysis of epidemiological studies, clinical reports, and public health surveillance data. Data on HTLV‐1 prevalence, incidence, clinical outcomes, proviral load associations, and public health measures were extracted and compared across major endemic and nonendemic regions. HTLV‐1 exhibits extreme geographic heterogeneity. Hyperendemic foci include southwestern Japan (carrier population ∼534,000 in 2020), parts of Brazil (estimated 800,000 carriers), the Caribbean (e.g., Jamaica, general population prevalence ∼6.1%), and sub‐Saharan Africa (estimated 2–5 million infections, the largest global burden). In Central Australia, prevalence among Indigenous adults over 45 reaches 49.3%, the highest recorded regional rate globally. Prevalence varies significantly within populations: In Brazil, it is highest in the north/northeast. In Gabon, rural prevalence is 8.7%, rising to 12.5% in rainforest provinces, with Pygmy ethnicity identified as an independent risk factor. In Iran, prevalence is concentrated in the northeast (2%–7%), whereas the rest of the country shows rates below 1%. In contrast, prevalence is very low in nonendemic areas such as the United States and most of Europe (< 0.01% in Spain and Italy), except for Romania (5.3 per 10,000 donors) and areas with migrant populations. Incidence data are sparse but informative: In Japan, the annual incidence among blood donors is 6.88 per 100,000 person‐years for women and 2.29 per 100,000 person‐years for men. In the United Kingdom, the incidence of HAM/TSP among HTLV‐1 carriers is 1.98 per 1000 person‐years. A Brazilian cohort reported an HAM/TSP incidence of 1.47% over 3 years, substantially higher than Japan’s lifetime risk of 0.25%. HTLV‐1 remains a significant yet profoundly neglected global pathogen, exhibiting extreme geographic heterogeneity in prevalence, clinical outcomes, and transmission dynamics, driven by complex interactions of viral genetics, host factors, and disparities in public health infrastructure. Although proven cost‐effective interventions such as universal antenatal screening in Japan have demonstrably reduced transmission, the persistent “silent” spread in endemic, low‐resource regions particularly sub‐Saharan Africa and Indigenous Australia demonstrates a critical global health inequity demanding urgent, region‐specific strategies for screening, prevention, and patient care to mitigate its substantial burden of morbidity and mortality.

## Linked entities

- **Diseases:** adult T-cell leukemia/lymphoma (MONDO:0019471), HTLV-1-associated myelopathy/tropical spastic paraparesis (MONDO:0008039)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** Rex [NCBI Gene 1491937], BCL2L1 (BCL2 like 1) [NCBI Gene 598] {aka BCL-XL/S, BCL2L, BCLX, Bcl-X, PPP1R52}, gag [NCBI Gene 1491934], POLE4 (DNA polymerase epsilon 4, accessory subunit) [NCBI Gene 56655] {aka YHHQ1, p12}, CADM1 (cell adhesion molecule 1) [NCBI Gene 23705] {aka BL2, IGSF4, IGSF4A, NECL2, Necl-2, RA175}, CREB1 (cAMP responsive element binding protein 1) [NCBI Gene 1385] {aka CREB, CREB-1}, CNTN2 (contactin 2) [NCBI Gene 6900] {aka AXT, EPEO5, FAME5, TAG-1, TAX, TAX1}, HBZ (hemoglobin subunit zeta) [NCBI Gene 3050] {aka HBAZ, HBZ-T1, HBZ1}, CD7 (CD7 molecule) [NCBI Gene 924] {aka GP40, LEU-9, TP41, Tp40}, HLA-C (major histocompatibility complex, class I, C) [NCBI Gene 3107] {aka D6S204, HLA-JY3, HLAC, HLC-C, MHC, PSORS1}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, IL15 (interleukin 15) [NCBI Gene 3600] {aka IL-15}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, H3P6 (H3 histone pseudogene 6) [NCBI Gene 440926] {aka H3F3AP4, p13}, JUNB (JunB proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 3726] {aka AP-1}, HLA-DRB1 (major histocompatibility complex, class II, DR beta 1) [NCBI Gene 3123] {aka DRB1, HLA-DR1B, HLA-DRB, SS1}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, HLA-B (major histocompatibility complex, class I, B) [NCBI Gene 3106] {aka AS, B-4901, HLAB}, CENPV (centromere protein V) [NCBI Gene 201161] {aka 3110013H01Rik, CENP-V, PRR6, p30}, HLA-A (major histocompatibility complex, class I, A) [NCBI Gene 3105] {aka HLAA}, IFNA1 (interferon alpha 1) [NCBI Gene 3439] {aka IFL, IFN, IFN-ALPHA, IFN-alphaD, IFNA13, IFNA@}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, HLA-DQB1 (major histocompatibility complex, class II, DQ beta 1) [NCBI Gene 3119] {aka CELIAC1, HLA-DQB, IDDM1}
- **Diseases:** Skin problems (MESH:D012871), strongyloidiasis (MESH:D013322), bronchiectasis (MESH:D001987), leukemia/lymphoma (MESH:D007938), neutropenia (MESH:D009503), warts (MESH:D014860), death (MESH:D003643), eczema (MESH:D004485), HTLV-1 (MESH:D015490), syphilis (MESH:D013587), RA (MESH:D001172), leprosy (MESH:D007918), PVL (MESH:C536761), retinal vasculitis (MESH:D031300), inflammatory (MESH:D007249), arthritis (MESH:D001168), floaters (MESH:C000726608), liver disease (MESH:D008107), diseases (MESH:D004194), MTCT (MESH:C562515), ATL (MESH:D015459), HAM (MESH:D015493), HBV/HCV infections (MESH:D006509), leukocytosis (MESH:D007964), extrapulmonary tuberculosis (MESH:D000092225), chorioretinal lesions (MESH:D002825), dehydration (MESH:D003681), polymyositis (MESH:D017285), Hypercalcemia (MESH:D006934), Sjogren's syndrome (MESH:D012859), cancer (MESH:D009369), opportunistic infections (MESH:D009894), cytogenetic abnormalities (MESH:D002869), lower-limb weakness (MESH:D018908), skin thickening (MESH:D013585), diabetes (MESH:D003920), bone marrow infiltration (MESH:D001855), sensory disturbances (MESH:D012678), cardiovascular disease (MESH:D002318), maculopapular eruptions (MESH:D003875), urinary hesitancy (MESH:D014548), peripheral T-cell lymphomas (MESH:D016411), Infections (MESH:D007239), impaired (MESH:D060825), STI (MESH:D012749), tuberculosis (MESH:D014376), pneumonia (MESH:D011014), parasitic infection (MESH:D010272), HIV-seropositive (MESH:D006679), CD4+ T-cell malignancy (MESH:D018344), diarrhea (MESH:D003967), uveitis (MESH:D014605), paresthesia (MESH:D010292), esophageal candidiasis (MESH:D002177), dermatitis (MESH:D003872), autoimmune manifestations (MESH:D012877), chronic lung disease (MESH:D029424), neurological disease (MESH:D020271), dengue (MESH:D003715), spastic gait (MESH:D020233)
- **Chemicals:** AZT (MESH:D015215), anthracycline (MESH:D018943), arsenic trioxide (MESH:D000077237), methimazole (MESH:D008713)
- **Species:** hepatitis C virus [taxon 11103], Homo sapiens (human, species) [taxon 9606], Primates (primates, order) [taxon 9443], Hungerfordia sp. U (species) [taxon 563713], Strongyloides stercoralis (species) [taxon 6248], Human T-cell leukemia virus type I (no rank) [taxon 11908], Mycobacterium tuberculosis (species) [taxon 1773], Human immunodeficiency virus 1 (no rank) [taxon 11676], Human T-lymphotropic virus 2 (no rank) [taxon 11909]

## Full text

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## References

231 references — full list in the complete paper: https://tomesphere.com/paper/PMC12927918/full.md

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Source: https://tomesphere.com/paper/PMC12927918