Related Experiment Videos
Laboratory test differences associated with HTLV-I and HTLV-II infection. Retrovirus Epidemiology Donor Study
E L Murphy1, S Glynn, K Watanabe
1University of California San Francisco 94143-0884, USA. murphy@labmed.ucsf.edu
Summary
Laboratory abnormalities in Human T-lymphotropic virus (HTLV-I and HTLV-II) are inconsistent. This study found HTLV-I and HTLV-II infections are associated with higher lymphocyte and platelet counts in blood donors.
Area of Science:
- Hematology
- Virology
- Immunology
Background:
- Inconsistencies exist in reported laboratory abnormalities linked to Human T-lymphotropic virus type I (HTLV-I) and type II (HTLV-II) infections.
- Understanding these hematological changes is crucial for diagnosing and managing HTLV infections.
Purpose of the Study:
- To investigate and quantify laboratory abnormalities in HTLV-I and HTLV-II infected individuals.
- To compare hematological and serum chemistry measures between seropositive and seronegative blood donors.
Main Methods:
- A cohort study involving 153 HTLV-I, 386 HTLV-II, and 795 HTLV-seronegative blood donors.
- Complete blood counts and selected serum chemistry measures were assessed.
- Linear and logistic regression analyses adjusted for confounding variables like age, gender, race, education, blood center, and injection drug use.
Main Results:
- HTLV-I and HTLV-II infected donors showed significantly higher absolute lymphocyte counts (6% and 10% increase, respectively).
- Both HTLV-I and HTLV-II seropositive donors had elevated platelet counts (average increase of 17,630 and 15,160, respectively).
- HTLV-I infection was associated with lower eosinophils and higher lactic dehydrogenase, while HTLV-II infection showed decreased creatine kinase, increased mean corpuscular volume, and lower serum calcium.
Conclusions:
- Both HTLV-I and HTLV-II infections are associated with increased lymphocyte and platelet levels through unknown mechanisms.
- Lower eosinophil counts in HTLV-I infection may correlate with increased susceptibility to parasitic diseases.