Thrombotic Thrombocytopaenic Purpura (TTP)


image_pdfimage_print

Endothelium-DamageThrombotic thrombocytopaenic purpura (TTP) is a pentad of neurological symptoms, pyrexia, renal dysfunction and microangiopathic haemolytic anaemia with thrombocytopaenia. The platelet microthrombi which form in the microcirculation are responsible for most symptoms seen in this condition due to resulting organ ischaemia. The endothelia of the kidneys, brain, heart, pancreas, spleen, and adrenal glands are particularly vulnerable to TTP. While the liver, lungs, gastrointestinal tract, gallbladder, skeletal muscles, retina, pituitary gland, ovaries, uterus,and testes are affected to a lesser extent.

Ensynthesis-of-von-willebrand-factordothelium Damage

To better understand the pathophysiology of TTP it is important to first understand platelet function, the role of von Willebrand Factor (vWF) and the proteolytic enzyme ADAMTS13, when endothelium is injured. During this process platelets play an essential role in orchestrating the blood clotting processes necessary to seal breaches in damaged blood vessels.  Recruitment and activation of platelets at sites of endothelium damage is dependent on vWF, which is synthesized by endothelial cells. The endothelial cells located near the site of damage respond by producing vWF which is secreted in the form of llarge multimeric chains.

Preteolytic-cleavage-of-von-willebrand-factorProteolytic Cleavage of von Willebrand Factor

The cleaved fragments of vWF bind to the exposed subendothelial collagen. Platelets express cell surface receptors, such as GP1b, that allows them to detect and adhere to vWF bound to collagen fibrils. In addition platelets express cell surface receptors, such as GPIIb/IIIa, that mediates platelet binding to other platelets via fibrinogen intermediates.

adhesion-of-von-willebrand-factorAdhesion of von Willebrand Factor

These factors contribute to recruitment of platelets to the site of endothelium damage and platelet aggregation that forms a seal in the breached endothelium. The platelets also initiates the blood clotting cascade that generates a meshwork of insoluble fibrin.

aggregation-of-plateletsWhat is thrombotic thrombocytopaenic purpura (TTP)?
In TTP, the plasma-derived proteolytic enzyme ADAMTS13, that cleaves the large multimeric chains of von Willebrand factor into smaller fragments, is depleted due to the presence of an autoantibody.

Thrombotic-thrombocytopaenic-purpurautoantibodies can be produced through molecular mimicry following a humoral response to an infection or by disruption of tolerance to self-antigens. This is observed in autoimmune diseases like SLE or during HIV infection. During HIV infection, there is both disruption of CD4+ T cell regulation and an increased risk of opportunistic infections. There is thus a greater likelihood of autoantibody generation through molecular mimicry. Because in this case, our patient was HIV infected, there was a strong likelihood that the action of ADAMST13 was inhibited, or neutralized, by the formation of autoantibodies.

TTP can also occur during pregnancy and may be related to the increased risk of developing autoantibodies when immune responses are polarized towards a Th2 cytokine profile, which favours development of humoral immunity.

In the absence of ADAMTS13 proteolytic activity, the large chains of vWF multimers are increased in the circulation and bind to exposed subendothelial collagen fibrils, initiating recruitment of large numbers of platelets to sites of endothelium damage.

Thrombotic-thrombocytopaenic-purpura2Due to the size and number of these chains excessive numbers of platelets are recruited and activated, resulting in:

Platelet depletion or thrombocytopaenia
Impedence of red cells through small blood vessels causing cells to shear with a resulting             microangiopathic haemolytic anaemia (MAHA) and organ ischaemia
Fragments of erythrocytes are visible in blood smears and are known as schistocytes.

Treatment of TTP
The diagnosis of TTP is essentially a clinical diagnosis. Although not all 5 criteria listed in the pentad are always present, life saving treatment is often initiated on the evidence of MAHA alone.

TTP can be treated by plasma infusion or exchange therapy which provides the missing enzyme ADAMTS13 and restores proteolytic cleavage of the large multimeric chains of vWF into smaller fragments, thus avoiding excessive platelet aggregation in small blood vessels. Plasma exchange therapy additionally contributes to the reduction or removal of the autoantibodies to ADAMTS13 by diluting them out.

Plasma-InfusionRituximab Therapy
In some cases plasma infusion or exchange therapy fails to provide a long-term benefit. This is found where the inhibition of ADAMTS13 is due to the persistence of autoantibody producing B lymphocytes that are not removed by plasma treatment. In these circumstances treatment with rituximab should be considered. This is a CD20 binding monoclonal antibody that selectively binds to B lymphocytes and mediates their destruction. Removal of the source of the autoantibody, results in restoration of significant ADAMTS13 activity.

Rituximab-therapy

Download combined PDF of Platelet Activation Graphics

Download combined PDF of Thrombotic Thrombocytopaenic Purpura Graphics

Link to the Associated Case Study

Return to the Case Study Discussion Page

 
 
 
 
 
 
International Union of Immunological SocietiesUniversity of South AfricaInstitute of Infectious Disease and Molecular MedicineScience Education PrizesElizabeth Glazer Pediatric Aids FoundationAlere