Are activated lymphocytes present in malaria and typhoid fever?

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Activated Lymphocytes in Malaria and Typhoid Fever

Yes, activated lymphocytes are present in both malaria and typhoid fever, though the patterns differ significantly between these two infections.

Lymphocyte Activation in Typhoid Fever

Typhoid fever demonstrates clear evidence of lymphocyte activation with characteristic alterations in T-cell populations. Research shows that patients with typhoid fever have increased lymphocyte adenosine deaminase (L-ADA) activity, which serves as a marker of immune response and lymphocyte activation 1. This enzymatic increase is prolonged and persists despite treatment, directly correlating with the immune response 1.

T-Cell Subset Alterations

  • The ratio of T lymphocyte subpopulations becomes grossly imbalanced in typhoid patients, with significant changes in T cells bearing receptors for IgM (Tμ) and IgG (Tγ) 2.

  • Complicated cases of typhoid fever show more severe alterations in T lymphocyte numbers and subpopulations compared to uncomplicated cases 2.

  • Cell-mediated immune response (CMIR) remains intact in uncomplicated typhoid cases but becomes depressed in complicated cases, suggesting that the imbalance within T lymphocyte subsets is responsible for this immunosuppression 2.

  • The presence of activated lymphocytes and intact CMIR may be more critical for recovery in typhoid fever than specific antibody production 2.

Lymphocyte Activation in Malaria

While the provided guidelines focus primarily on clinical and laboratory diagnostic features of malaria rather than specific cellular immune responses, malaria is well-established to trigger significant lymphocyte activation as part of the host immune response. The clinical guidelines emphasize that:

  • Lymphopenia is common in malaria, particularly in severe cases and with certain viral co-infections like dengue and HIV 3.

  • Thrombocytopenia (<150,000/μL) is the most frequent laboratory finding in malaria, occurring in 70-79% of patients regardless of Plasmodium species 3.

Clinical Differentiation

Key Laboratory Findings

  • In malaria: Thrombocytopenia (positive likelihood ratio 5.6-11.0), hyperbilirubinemia (positive likelihood ratio 5.3-7.3), and lymphopenia are characteristic 3.

  • In typhoid fever: Lymphopenia is common, with blood cultures showing 80% sensitivity in the first week 3.

Diagnostic Pitfalls

A critical caveat is that co-infection with malaria and typhoid can occur, particularly in endemic regions like Malaysia, India, and Cameroon 4, 5. However, the number of cases diagnosed as concurrent malaria-typhoid infection is frequently overestimated when relying solely on serological tests 5, 6. One study found that only 17% of patients had true concurrent infection based on bacteriological diagnosis, compared to 47.9% based on Widal test alone 5.

Practical Approach

  • Always exclude malaria first in any febrile patient returning from tropical areas, as it is the most important potentially fatal cause 7, 8.

  • Obtain blood cultures before initiating antibiotics for suspected typhoid fever, as they are the gold standard for diagnosis 7.

  • Do not rely solely on Widal testing or malaria antibody card tests for diagnosing co-infection, as these have high false-positive rates 5, 6.

  • Confirmed co-infection rates are much lower (1.6%) than suggested by serological testing alone 6.

References

Research

Increased lymphocyte adenosine deaminase in typhoid fever.

Scandinavian journal of infectious diseases, 1981

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

An update on concurrent malaria and typhoid fever in Cameroon.

Transactions of the Royal Society of Tropical Medicine and Hygiene, 1999

Guideline

Enteric Fever and Pulmonary Complications

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Tropical Infections Causing Jaundice and Elevated Transaminases

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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