The α-gal Syndrome - Investigating Immune Reactions to Tick Bites Leading to Inflammation and Allergic Sensitization

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

The goal of this clinical trial is to follow immune response and antibody build-up in individuals bitten by a tick. Participants are invited to enroll within 48 hours after the tick removal and donate some blood. The tick is also collected and analysed. Researchers will then try to answer the following questions: * Was the tick infected with parasites? * How many infected ticks actually transmitted the parasites to the host? * Did the participant make antibodies against tick proteins or tick-borne parasites? * Did the participant develop IgE antibodies against the alpha-Gal sugar? The alpha-Gal sugar is present on mammalian meat, and ticks can transmit the alpha-Gal sugar to the host during their blood meal. Humans recognize the alpha-Gal sugar as foreign and some individuals will build IgE antibodies in response. These IgE antibodies against alpha-Gal can lead to a food allergy to red meat, also known as alpha-Gal syndrome. Researchers will compare a group of participants that develop IgE against the alpha-Gal sugar with participants that will not. They want to find out if there are specific cells or mechanisms that differentiate the 2 groups. Participants will: * Enroll after a recent tick bite or within 48 hours after tick removal: they will be asked to donate some blood and fill out a questionnaire. * Visit the clinic 4 to 6 weeks later for a follow-up sample and questionnaire. * Visit the clinic 3 months after the tick bite for allergy tests if they have been selected for this 3rd visit.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• Individuals aged ≥ 18 years, Male and Female.

• Experience of a tick bite: the tick has been removed less than 48 hours ago, or the tick is still attached to the skin and can be removed on site by the study nurse.

• Tick available for analysis.

• Informed consent signed.

Locations
Other Locations
Luxembourg
LCTR
RECRUITING
Luxembourg
Time Frame
Start Date: 2025-07-01
Estimated Completion Date: 2027-02
Participants
Target number of participants: 100
Treatments
a-Gal sensitized participants
Following the second visit 4 to 6 weeks after the tick bite, participants with specific alpha-Gal IgE levels above 0.1 kU/L are assigned to this group of a-Gal sensitized participants.
a-Gal non-sensitized participants
Following the second visit 4 to 6 weeks after the tick bite, participants with specific alpha-Gal IgE levels below 0.1 kU/L are assigned to this group of a-Gal non-sensitized participants.
Related Therapeutic Areas
Sponsors
Collaborators: Centre Hospitalier du Luxembourg, Luxembourg National Research Fund (FNR)
Leads: Luxembourg Institute of Health

This content was sourced from clinicaltrials.gov

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