Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID06612515

Prospective Cohort Study Investigating Vaccine-Induced Immune Responses Against Respiratory Viral Infections in Immunocompromised Patients With or Without Hematological Conditions

Led by University of Cologne · Updated on 2026-05-12

1000

Participants Needed

1

Research Sites

35 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying the immune responses to vaccines against respiratory viruses in immunocompromised patients, including those with hematological or oncological conditions. These patients often have weakened immune systems due to disease or treatment, making them more vulnerable to severe respiratory infections from viruses like influenza, RSV, and coronaviruses. The study aims to better understand how vaccine-induced immunity, especially T cell responses, functions in these patients, as current data mostly focuses on antibody responses which may be less effective in this group. This observational study will analyze early and late booster vaccinations in immunocompromised patients who are vaccinated as part of routine care. It will focus on measuring virus-specific T cell responses and humoral immune responses over time. The research will gather blood samples and other data to assess the cellular and antibody responses to vaccination, helping to fill knowledge gaps about long-term protection in this vulnerable population. Participants will be monitored for up to 12 months after vaccination to evaluate humoral and cellular immune responses, including seroconversion. The study will collect and analyze samples at various points to measure these immune markers. The University of Cologne leads this research, which seeks to improve understanding of vaccine effectiveness and guide better preventive strategies for immunocompromised patients facing respiratory viral infections.

CONDITIONS

Brief Title

Vaccine-induced Immunity in Immunocompromised Patients

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Signed informed consent form
  • Patients with immunosuppression caused by treatment or underlying diseases
  • Patients who have been vaccinated or are willing to be vaccinated against respiratory virus infections according to current recommendations
  • Age 18 years or older
Not Eligible

You will not qualify if you...

  • Patients unwilling or ineligible for vaccination under current recommendations

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surveillance

Duration - 12 months

Participants who undergo routine vaccination and care are observed for immune responses to respiratory virus vaccines.

Multiple visits for sample collection and immune response assessments

Trial Site Locations

Total: 1 location

1

University Hospital Cologne

Cologne, North Rhine-Westphalia, Germany, 50937

Actively Recruiting

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Research Team

S

Sibylle Mellinghoff, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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