# Trypanosoma-Cruzi Cross-Reactive Antibodies Longitudinal Follow-Up: A Prospective Observational Study in Hematopoietic Stem Cell Transplantation

**Authors:** Esber S. Saba, Lucie Gueyffier, Marie-Laure Danjoy, Philippe Vanhems, Bruno Pozzetto, Mohamad Sobh, Hans Pottel, Mauricette Michallet, Maan A. Zrein

PMC · DOI: 10.1371/journal.pone.0137240 · PLoS ONE · 2015-09-09

## TL;DR

This study tracks TcCRA antibodies in stem cell transplant patients to see if they can be transmitted from donors to recipients.

## Contribution

The study provides new insights into the transmission dynamics of TcCRA antibodies through allogeneic hematopoietic stem cell transplantation.

## Key findings

- TcCRA seroconversion occurred in 4 out of 24 recipients from TcCRA-positive donors.
- No seroconversion was observed in recipients from TcCRA-negative donors.
- The study suggests TcCRA may be passively or actively transmitted through stem cell transplantation.

## Abstract

Antibodies named TcCRA “Trypanosoma cruzi Cross Reactive Antibodies” were detected in 47% of blood donors from French population unexposed to the parasite. In order to evaluate the passive or active transmissibility of TcCRA and further characterize its role and etiology, we have conducted a study in a cohort of 47 patients who underwent allogeneic Hematopoietic Stem Cell Transplantations (allo-HSCT). Donors and recipients were tested for TcCRA prior to transplantation. Recipients were further tested during follow-up after transplantation. Demographical, clinical and biological data were collected. Our primary end-point was to assess the risk of TcCRA acquisition after transplantation. During this initial analysis, we observed no seroconversion in patients receiving cells from TcCRA negative donors (n = 23) but detected seroconversion in 4 out of 24 patients who received hematopoietic stem cells from positive donors. Here, we are discussing possible scenarios to explain TcCRA-immune status in recipient after transplantation.

## Full-text entities

- **Genes:** HLA-A (major histocompatibility complex, class I, A) [NCBI Gene 3105] {aka HLAA}
- **Diseases:** Hodgkin's lymphoma (MESH:D006689), cancer (MESH:D009369), poliomyelitis (MESH:D011051), hematological malignancies (MESH:D019337), measles (MESH:D008457), bone marrow failure (MESH:D000080983), herpes (MESH:C536395), MA (OMIM:157300), opportunistic infection (MESH:D009894), Chagas disease (MESH:D014355), aplasia (MESH:C536482), infectious (MESH:D003141), EBV (MESH:D020031), Toxoplasmosis (MESH:D014123), mumps (MESH:D009107), CMV (MESH:D003586), Myeloproliferative syndrome (MESH:D009196), acute lymphoblastic and myeloid leukemia (MESH:D054198), died (MESH:D003643), CMV viremia (MESH:D014766), non-Hodgkin's lymphoma (MESH:D008228), CMV reactivation (MESH:D000085343), infection (MESH:D007239), GVHD (MESH:D006086), rubella (MESH:D012409)
- **Species:** Human betaherpesvirus 6 (species) [taxon 10368], Human alphaherpesvirus 1 (Herpes simplex virus type 1, no rank) [taxon 10298], Homo sapiens (human, species) [taxon 9606], human gammaherpesvirus 4 (Epstein Barr virus, no rank) [taxon 10376], Measles morbillivirus (no rank) [taxon 11234], Marseillevirus marseillevirus (no rank) [taxon 694581], mumps virus [taxon 1979165], Trypanosoma cruzi (species) [taxon 5693], Human alphaherpesvirus 3 (Varicella-zoster virus, no rank) [taxon 10335]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC4564178/full.md

## References

16 references — full list in the complete paper: https://tomesphere.com/paper/PMC4564178/full.md

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Source: https://tomesphere.com/paper/PMC4564178