Blood clot helps ECM formation and remodeling, material-dependent.
Cells remodel blood clot, make pockets where they make new tissue.
Fibroblasts are active in the chronic inflammation phase.
Material-specific macrophage secretome, which are cytokines secreted by macrophages, result in fibroblast chemotaxis and ECM formation.
Dynamic models, such as bioreactors, control hemodynamic conditions which affect the inflammatory state by shear stresses and cyclic strains.
The inflammatory state regulates the tissue formation.
Host response of a man ≠ woman ≠ newborn ≠ infant ≠ elderly indicates that personalized treatment isneeded.
Ageing is associated with immunosenescence and disturbed redox balance.
Dysfunctional immune system is a characteristic of ageing.
Ageing increases the risk of thrombosis.
Ageing increases the risk of infection.
Ageing impairs wound healing.
Patient-specific characteristics are poorly studied, both in vivo and in vitro.
Inter species differences, for example between mice, rats, sheep, and humans, need to be considered.
Hypothesis driven animal research is common in the field of biomaterials.
Human in vitro models are often oversimplified and strongly reductionist, focusing on cytokine/GF secretion and ECM formation.
Human in vitro models are accessible but lack the complexity and throughput of native-like models.
Biomaterials are materials that have an interaction with your body.
The response to biomaterials has to be studied for device safety.
There are many problems that can occur during the interaction of biomaterials with the body: local interactions, systemic interactions and device- patient complications.
Immunomodulatory biomaterials cannot be considered as inert, as they cannot be hidden from the immune system.
The host response is not always bad, it needs to be controlled.
The inflammation in the beginning is necessary to kick start the healing process.
Biomaterials can interact with/instruct the immune system.
There are materials that induce tissue regeneration, which work on the innate immune system.
There are also materials to silence/activate immune cells, which work on the adaptive immune system.
Biomaterial applications include replacement (permanent) implants and regenerative (degradable) implants, which have different effects on the immune system.
Biocompatibility is the ability of a material to perform with an appropriate host response in a specific application.
Biotolerability is the ability of materials to reside in the body for long periods of time with only low degrees of inflammatory reaction.
Factors that influence the host-response include biomaterial-related factors such as composition, material, degradability, mechanical properties, sterility, antigenicity and active ingredients (drugs).
Host-related factors that influence the host-response include age, gender, anatomic location, previous interventions, comorbidities, immune response and medications.
The first line of defense in the immune system is mechanical barriers such as a mosquito breaking through.
The second line of defense in the immune system is the innate immune system.
The third line of defense in the immune system is the adaptive immune system.
Immune cells move from the vasculature to the parasites in the innate immune system.
Innate immune system is nonspecific and responds quickly.
Biomaterials mainly trigger the innate immune response, they are typically not antigenic (adaptive).
Adaptive immune system is specific and involves antigen presentation, it responds slowly the first time but has a memory.