- Research article
- Open Access
- Open Peer Review
HTLV-1 infection in solid organ transplant donors and recipients in Spain
BMC Infectious Diseasesvolume 19, Article number: 706 (2019)
HTLV-1 infection is a neglected disease, despite infecting 10–15 million people worldwide and severe illnesses develop in 10% of carriers lifelong. Acknowledging a greater risk for developing HTLV-1 associated illnesses due to immunosuppression, screening is being widely considered in the transplantation setting. Herein, we report the experience with universal HTLV testing of donors and recipients of solid organ transplants in a survey conducted in Spain.
All hospitals belonging to the Spanish HTLV network were invited to participate in the study. Briefly, HTLV antibody screening was performed retrospectively in all specimens collected from solid organ donors and recipients attended since the year 2008.
A total of 5751 individuals were tested for HTLV antibodies at 8 sites. Donors represented 2312 (42.2%), of whom 17 (0.3%) were living kidney donors. The remaining 3439 (59.8%) were recipients. Spaniards represented nearly 80%.
Overall, 9 individuals (0.16%) were initially reactive for HTLV antibodies. Six were donors and 3 were recipients. Using confirmatory tests, HTLV-1 could be confirmed in only two donors, one Spaniard and another from Colombia. Both kidneys of the Spaniard were inadvertently transplanted. Subacute myelopathy developed within 1 year in one recipient. The second recipient seroconverted for HTLV-1 but the kidney had to be removed soon due to rejection. Immunosuppression was stopped and 3 years later the patient remains in dialysis but otherwise asymptomatic.
The rate of HTLV-1 is low but not negligible in donors/recipients of solid organ transplants in Spain. Universal HTLV screening should be recommended in all donor and recipients of solid organ transplantation in Spain. Evidence is overwhelming for very high virus transmission and increased risk along with the rapid development of subacute myelopathy.
HTLV-1 infection is a neglected disease. As with other human retroviruses, i.e. HIV, acute infection is universally followed by long-lasting persistence of the virus. Clinical manifestations develop in roughly 10% of carriers lifelong, typically as subacute myelopathy which is known as tropical spastic paraparesis/HTLV-1-associated myelopathy (TSP/HAM)  or a lymphoproliferative disorder named adult T-cell leukaemia/lymphoma (ATLL) . Screening for HTLV antibodies is recommended in blood donors in some countries. Acknowledging a greater risk for developing HTLV-1 associated illnesses due to immunosuppression , screening of transplant donors and recipients is widely being encouraged .
Spain is leading solid organ transplantation worldwide. With 47 million people, 5261 transplants were performed in 2017 (kidney 3269), liver (1247), lung (363) and heart (304). Overall it represents 20% of transplants within the European Union. Until recently, the Spanish law only recommended HTLV testing for persons with high epidemiological risk of infection . Herein, we report the experience with universal testing of a large population of donors and recipients of solid organ transplants in Spain.
A nationwide network of hospitals/clinics/labs was set up in Spain in 1989 and a national register of HTLV-1 cases works since then. Currently, more than 50 centres distributed across the Spanish geography belong to this group. Further information on this network has been reported elsewhere . All hospitals were invited to participate in the current study. Briefly, HTLV antibody screening using chemiluminescence and/or ELISA of all solid organ donors and recipients attended since 2008 was retrospectively analyzed.
All numerical variables are reported as absolute values and percentages. Categorical variables were compared using χ2 or Fisher exact tests whereas non-categorical variables were compared using Student T-test or Mann-Whitney U tests. All analyses were 2-tailed and only p values below 0.05 were considered as significant. All statistical analyses were performed using SPSS software version 16.0 (SPSS Inc., Chicago, IL).
A total of 5751 individuals were tested for HTLV antibodies at 8 sites. Table 1 records the main characteristics of the study population. Donors represented 2312 (42.2%), of whom only 17 (0.3%) were living kidney donors. The remaining 3439 (59.8%) were recipients. Males were predominant (59.7%). The median age was 57-years old. Spaniards represented nearly 80%, being Latin Americans only 65 (1.1%) and Africans 101 (1.8%). Overall, transplant recipients were more frequently male, younger, and native Spaniards than organ donors.
Overall, 9 individuals were initially reactive for HTLV antibodies. Table 2 summarizes the main characteristics of these patients. Six were donors and 3 were recipients. Using confirmatory tests (western blot and PCR), HTLV-1 was found in only two patients. Another three were positive for HTLV-2. Two samples gave indeterminate results and another two were negative.
The two HTLV-1 positive cases were donors. Thus, the overall rate of HTLV-1 among solid transplant donors in our study was 0.09%. The first individual was a 49-year old female, born in Colombia, diagnosed in 2015, at the time she was assessed to be a kidney living donor. Before moving to the surgical procedure, she was discharged as potential donor following knowledge of her HTLV-1 seropositive status.
The second HTLV-1 case was a 38-year old male, born in Spain, that died in 2015. Both kidneys were inadvertently transplanted. TSP/HAM developed within 1 year in one recipient, despite antiretroviral prophylaxis attempted within the first weeks. The second recipient seroconverted for HTLV-1 but the kidney had to be removed soon due to rejection. Immunosuppression was stopped and to date, 3 years later, the patient remains in dialysis but otherwise asymptomatic.
The three HTLV-2 cases were two donors and one recipient. All had been born in Spain. The last patient died before transplantation. The two donors were finally discharged from transplantation because they were also positive for HIV and hepatitis C.
More than 35 years after the discovery of HTLV-1 , donor/recipient screening for the virus remains sporadic or non-existent in most countries. In 1993, the American CDC recommended that persons infected with HTLV be counselled “not to donate blood, semen, body organs or other tissues” . Nevertheless, in the year 2009 the recommendation for universal HTLV screening in deceased organ donors was dropped in the United States because of the perception of low HTLV-1 prevalence and low positive predictive value of serologic screening tests . Alongside this recommendation, most international transplant society guidelines currently do not provide any advice on HTLV-1 screening and use of donated organs.
High rates of HTLV-1 have been found in specific groups in non-endemic regions of North America  and Europe , and decades of migration/immigration and tourism/travelling have altered the demographics of many Western countries. For example, the ongoing refugee migration from the Middle East and Africa would rapidly change the prevalence of HTLV-1 in many European countries. For a while this has been the case with Latin Americans in Spain, given the large flux of immigration facilitated by strong cultural and ancestor links .
Since the year 1988 there is a national register of HTLV-1 cases in Spain. A total of 369 cases had been reported until December 2018. Most cases are concentrated around the largest urban areas (Madrid and Barcelona) where the greatest immigrant populations are living. However, HTLV-1-infected persons have been identified across the whole Spanish geography. Although many were immigrants from endemic areas, mostly in Latin America, up to 18% were native Spaniards .
The rapid development of subacute myelopathy was seen in one of our recipients from a kidney from the HTLV-1 positive cadaveric donor. Similar cases of subacute myelopathy shortly after transplantation have already been reported in the literature [12,13,14], including a series of recipients from a single donor in Spain . Myelopathy was originally reported in a heart transplant recipient in France following HTLV-1 acquisition from contaminated blood transfusions during the surgery . Transplant immunosuppression seems to play a major role in the accelerated disease progression in this setting .
In response to the worldwide evolving foci of HTLV-1 infections and the very poor prognosis of post-transplant virus-associated illnesses, there are urgent calls for a broader HTLV-1 screening of live and -more difficult- deceased organ donors. Organ procurement organizations and transplant programs should determine local prevalence to guide HTLV-1 screening efforts . Targeted screening of potential high-risk living (and deceased) donors for HTLV-1 has been recommended by some authors . Suggestions also have been put forward for national or international registries of all HTLV-1-affected transplants . Alerted to the dangers of rapid-onset TSP following HTLV-1-infected organ transplants, Japan began in 2014 screening for HTLV-1 of all kidney donations. Similarly, the United Kingdom issued new transplantation guidance on HTLV-1 screening of cadaveric solid organs in 2011. Finally, the Global Virus Network has recently called for more systematic HTLV-1 screening before solid organ transplantation everywhere .
The screening costs for HTLV-1 are small in comparison with the cost of post-transplant illnesses and/or death associated with TSP or ATL following HTLV-1 infection . For all these reasons, the American and European CDCs along with other health prevention agencies should urgently update their policy recommendations on organ transplant HTLV-1 screening. In the meantime, some transplant centres around the world, including a few in Spain, have already implemented “rapid” (or “urgent”) HTLV-1 testing of all deceased organ donors. In parallel, diagnostic companies should design rapid tools (i.e., point-of-care (PIC) assays) and improve the specificity of HTLV-1 screening tests to minimize unwanted organ discharge.
Our findings call into question the current view that anti-HTLV screening of donated organs is not needed or just recommended when there is suspicion, as it is recommended in Spain . This opinion is based on the assumption that HTLV-1-associated diseases will develop only in a small proportion of carriers and that progression to disease is slow compared with the average lifespan of humans and therefore poses no major threats to public health. In the transplant setting, the very high risk of transmission and the high rate along with short-term for developing HTLV-1 disease most likely results from immunosuppressive therapy.
We report a low but not negligible rate of HTLV-1 infection among donors and recipients of solid organ transplants in Spain. Of note, unaware HTLV-1-infected donors were not exclusively foreigners from highly endemic areas but native Spaniards that most likely have been exposed to HTLV-1 by sexual contact. Therefore, universal HTLV screening should be recommended in all donor and recipients of solid organ transplantation in Spain. Evidence is overwhelming for very high -if not uniform- virus transmission and increased risk as well as rapid disease progression, mostly subacute myelopathy.
Availability of data and materials
The Spanish HTLV database is a public registry ascribed to a public institution, Puerta de Hierro University Hospital, located in Madrid. The person responsible for granting access is Dr. Carmen de Mendoza, first author of this manuscript and current coordinator of the Spanish HTLV Network.
Center for Diseases Control and Prevention
Enzyme-linked immune serum assay
- HAM HTLV:
Human T lymphotropic virus type 1
Tropical spastic paraparesis
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We would like to thank all members of the HTLV Spanish Network.
C. Rodríguez, M. Vera & J. del Romero (Centro Sanitario Sandoval, Madrid); G. Marcaida & M.D. Ocete (Hospital General Universitario, Valencia); E. Caballero & I. Molina (Hospital Vall d’Hebrón, Barcelona); A. Aguilera, J.J. Rodríguez-Calviño, D. Navarro, C. Rivero & M.D. Vilariño (Hospital Conxo-CHUS, Santiago); R. Benito, S. Algarate & J. Gil (Hospital Clínico Universitario Lozano Blesa, Zaragoza); R. Ortiz de Lejarazu & S. Rojo (Hospital Clínico Universitario, Valladolid); J.M. Eirós & A. San Miguel (Hospital Rio Hortega, Valladolid); C. Manzardo & J.M. Miró (Hospital Clínic-IDIBAPS, Barcelona); J. García & I. Paz (Hospital Cristal-Piñor, Orense); E. Poveda (INIBIC-Complejo Hospitalario Universitario, A Coruña); E. Calderón (Hospital Virgen del Rocío & CIBERESP, Sevilla); D. Escudero (Hospital Germans Trias i Pujol, Barcelona); M. Trigo, J. Diz & M. García-Campello (Complejo Hospitalario, Pontevedra); M. Rodríguez-Iglesias (Hospital Universitario, Puerto Real); A. Hernández-Betancor & A.M. Martín (Hospital Insular Hospital Universitario, Las Palmas de Gran Canaria); J.M. Ramos & A. Gimeno (Hospital Universitario, Alicante); F. Gutiérrez, J.C. Rodríguez & V. Sánchez (Hospital General, Elche); C. Gómez-Hernando (Complejo Hospitalario Virgen de la Salud, Toledo); G. Cilla & E. Pérez-Trallero (Hospital Donostia, San Sebastián); J. López-Aldeguer (Hospital La Fe, Valencia); L. Fernández-Pereira (Hospital San Pedro de Alcántara, Cáceres); J. Niubó (Ciudad Sanitaria de Bellvitge, Barcelona); M. Hernández, A.M. López-Lirola & J.L. Gómez-Sirvent (Hospital Universitario La Laguna, Tenerife); L. Force (Hospital General, Mataró); C. Cifuentes (Hospital Son Llátzer, Palma de Mallorca); S. Pérez & L. Morano (Hospital do Meixoeiro, Vigo); C. Raya (Hospital del Bierzo, Ponferrada); A. González-Praetorius (Hospital Universitario, Guadalajara); J.L. Pérez & M. Peñaranda (Hospital Son Espases, Mallorca); S. Hernáez-Crespo (Hospital de Basurto, Bilbao); J.M. Montejo (Hospital de Cruces, Bilbao); L. Roc & A. Martínez-Sapiña (Hospital Miguel Servet, Zaragoza); I. Viciana (Hospital Virgen de la Victoria, Málaga); T. Cabezas, A. Lozano & J.M. Fernández (Hospital de Poniente, Almería); I. García-Bermejo & G. Gaspar (Hospital Universitario, Getafe); R. García, M. Górgolas, C. Vegas & J. Blas (Fundación Jiménez Díaz, Madrid); P. Miralles, M. Valeiro & T. Aldamiz (Hospital Gregorio Marañón, Madrid); N. Margall (Hospital Santa Creu i Sant Pau, Barcelona); C. Guardia & E. do Pico (ICS, Barcelona); I. Polo, A. Aguinaga & C. Ezpeleta (Complejo Hospitalario Navarra, Pamplona); S. Sauleda & M. Pirón (Banco de Sangre & Tejidos, Barcelona); R. González & L. Barea (Centro de Transfusiones, Madrid); A. Jiménez & L. Blanco (Centro de Hemoterapia y Hemodonación de Castilla y León, Valladolid); A. Suárez & I. Rodríguez-Avial (Hospital Clínico San Carlos, Madrid); A. Pérez-Rivilla, P. Parra & M. Fernández (Hospital Universitario 12 de Octubre, Madrid); M. Fernández-Alonso (Clínica Universitaria, Pamplona); A. Treviño, S. Requena, L. Benítez-Gutiérrez, V. Cuervas-Mons & C. de Mendoza (IIS Hospital Universitario Puerta de Hierro, Majadahonda); P. Barreiro (La Paz University Hospital, Madrid); V. Soriano, O. Corral & F. Gómez-Gallego (UNIR Health Sciences School & Medical Centre, Madrid).
Ethics approval and consent to participate
the study was approved by the hospital ethics committee of the reference center, Puerta de Hierro University Hospital. According to the normative in place, adherence to it was acknowledged by the Ethics committee of the remaining participating centres.
Consent for publication
All authors have read and approved the current submission.
The authors declare that they have no competing interests.
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