Article Text

Relapse of immune thrombotic thrombocytopenic purpura (iTTP) possibly triggered by COVID-19 vaccination and/or concurrent COVID-19 infection
Free
  1. Fei Fang1,
  2. Brandon Tse2 and
  3. Katerina Pavenski3,4
  1. 1Department of Medicine, University of Toronto, Toronto, Ontario, Canada
  2. 2Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada
  3. 3Departments of Medicine and Laboratory Medicine & Pathobiology, University of Toronto, Toronto, Ontario, Canada
  4. 4Departments of Laboratory Medicine and Medicine, St Michael's Hospital, Toronto, Ontario, Canada
  1. Correspondence to Dr Katerina Pavenski; katerina.pavenski{at}unityhealth.to

Abstract

Thrombotic thrombocytopenic purpura (TTP) is a life-threatening disease that may be triggered by inflammation, including infection or vaccination. Since the start of the COVID-19 pandemic, several case reports were published on de novo or relapsed immune TTP (iTTP) in COVID-19-infected patients. Case reports of iTTP episodes following vaccination against COVID-19 are also emerging. We report a case of relapsed iTTP in a patient who received Moderna mRNA-1273 SARS-CoV-2 vaccine and developed concurrent severe COVID-19 infection. The patient’s iTTP was successfully managed with caplacizumab, therapeutic plasma exchange and high-dose steroids. We summarise published cases of iTTP associated with COVID-19 infection or vaccination.

  • Thrombotic Thrombocytopenic purpura
  • COVID-19
  • Vaccination/immunisation

Statistics from Altmetric.com

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

Background

Immune thrombotic thrombocytopenic purpura (iTTP) is a rare, life-threatening disorder caused by severe ADAMTS13 deficiency due to autoantibodies and resulting in the accumulation of ultra-large von Willebrand factor (vWF) multimers and microvascular thrombi.1 Management includes therapeutic plasma exchange (TPE), immunosuppression and anti-vWF therapy.1

The role of ADAMTS13 and vWF in COVID-19 pathophysiology is not completely understood. Recent studies demonstrated an increased vWFAg/ADAMTS13 ratio, possibly driven by endothelial injury and excess ADAMTS13 consumption due to elevated vWF.2 This disruption of the ADAMTS13–vWF axis was associated with increased mortality in patients with COVID-19 in one study.3 However, another study found no pathological role for ADAMTS13 in COVID-19.4 Several cases of COVID-19-associated iTTP were reported,5–20 yet causation has not been demonstrated. iTTP following vaccination has been previously reported21 and cases of COVID-19 vaccine-associated iTTP are also emerging.22–25 We present a complicated case of relapsed iTTP following concurrent COVID-19 vaccination and infection.

Case presentation

A man in his 70s with a history of stroke, left ventricular aneurysm thrombosis (on chronic anticoagulation) and chronic kidney disease (baseline creatinine 130 µmol/L) presented with iTTP relapse. iTTP was first diagnosed 7 years ago, had no identifiable trigger and was complicated by refractoriness and severe acute kidney injury (AKI). He recovered following TPE, steroids and rituximab. He subsequently had three relapses, which were successfully treated with TPE and immunosuppression. He was well for the past 4 years and his remission ADAMTS13 activity was normal (71%).

The patient became unwell 7 days after his first dose of Moderna COVID-19 vaccine and 3–4 days after exposure to an individual infected with COVID-19. On admission to the hospital, the patient was febrile and dyspnoeic, with a chest X-ray (CXR) suggestive of left lower lobe pneumonia. Blood work (see table 1) revealed microangiopathic haemolytic anaemia, thrombocytopenia, AKI and elevated troponin. There were no neurological symptoms and CT of the head showed no acute abnormalities. On admission day 3, his oxygen requirements increased, necessitating transfer to the critical care for non-invasive respiratory support. On day 6, CXR revealed bilateral pneumonia (see figure 1) and the patient was intubated for severe respiratory failure.

Figure 1

Chest X-ray on day 6 of admission.

Table 1

Laboratory presentation on admission

Differential diagnosis

On admission, COVID-19 infection was suspected and the patient was placed in isolation. The initial COVID-19 nasopharyngeal swab was negative (Altona RealStar SARS-CoV-2 RT-PCR Kit 1.0). COVID-19 swab was repeated on day 6 and was positive. iTTP relapse was confirmed by undetectable ADAMTS13 activity and positive ADAMTS13 inhibitor (see table 1).

Treatment

Corticosteroids (1 mg/kg/day (day 1–20) followed by 10 mg/week taper) and TPE (1.0–1.5 plasma volume exchange with solvent detergent-treated plasma daily for 8 days) were started on presentation empirically. After confirmation of iTTP diagnosis, caplacizumab (anti-vWF nanobody) 11 mg once daily was added, while rituximab was deferred. The patient was also started on haemodialysis. Following confirmation of COVID-19 infection on day 6, he was switched to dexamethasone for a few days and then resumed on high-dose prednisone. Warfarin was held on admission; prophylactic dose low molecular weight heparin was started once platelets were above 30 000 and switched to therapeutic dose following platelet normalisation. The patient was subsequently resumed on warfarin. Fifteen doses of caplacizumab were given; caplacizumab was discontinued once clinical remission and ADAMTS13 activity over 10% were reached.

Outcome and follow-up

Treatment with TPE, corticosteroids, and caplacizumab induced a rapid and sustained clinical remission. No bleeding was noted with caplacizumab use. The patient developed deep vein thrombosis and several infections, including pulmonary aspergillosis. He underwent tracheostomy on day 24, was decannulated on day 47 and finally weaned off oxygen by day 58. Treatment of iTTP with rituximab (anti-CD20 antibody) was deferred due to concerns about exacerbating infections. The patient eventually recovered and was discharged from the hospital on day 74. Haemodialysis was discontinued and renal function returned to baseline by discharge. A few months later, he received rituximab (375 mg/m2 weekly for 4 weeks) for persistent severe ADAMTS13 deficiency (less than 10%) and his activity improved (34%). He eventually received the second dose of COVID-19 vaccine (Pfizer-BioNTech) without complications.

Discussion

iTTP is a life-threatening blood disease that may be triggered by immune response to infections, vaccinations and tissue injury.26 It is treated with TPE, immunosuppression and anti-vWF therapy.1 We described an iTTP relapse in a patient with recent COVID-19 vaccination and concurrent COVID-19 infection. The patient responded well to iTTP treatment, however, suffered significant complications of COVID-19. There were several unique features in this case. The patient presented with severe AKI during two of his iTTP episodes. Severe renal dysfunction necessitating renal replacement therapy is uncommon in iTTP.1 Following treatment, he returned to baseline kidney function both times. When added to TPE and immunosuppression, caplacizumab leads to faster platelet count response (HR, 1.65; p<0.001) and decreased refractoriness and mortality in iTTP.27 However, there are no studies on the safety of caplacizumab in patients on haemodialysis. Our patient received caplacizumab and tolerated it without any complications. Further studies on the safety of caplacizumab in patients with severe renal dysfunction are needed. Due to severe concurrent COVID-19 infection, rituximab was not administered. Rituximab is highly effective in treatment of antibody-mediated diseases such as iTTP.1 It causes rapid and sustained depletion of B cells, impairing humoral response to COVID-19 infection, and can potentially place patients at risk of reactivation or reinfection.28 Among reported cases of iTTP in patients with COVID-19,5–20 8 of 19 patients were treated with rituximab (see online supplemental table 2). Of these eight patients, three died; two of the deaths were due to COVID-19-related severe lung disease and multiorgan failure. It remains unclear whether immunosuppressive effect of rituximab could result in more severe COVID-19 and hence should be avoided during acute infection. Our team opted to delay rituximab and monitor for iTTP exacerbation. Considering the ongoing pandemic and the patient’s immunosuppressed state, we offered a second dose of COVID-19 vaccine. We debated the timing of the second dose, as well as using a different vaccine. However, the patient was worried about the vaccine triggering iTTP relapse and initially opted to defer the second dose.

Supplemental material

In our case, iTTP relapse occurred within 7 days of COVID-19 vaccination and 3–4 days post-COVID-19 exposure, after 4 years of remission. Timing of vaccination and exposure in this case, as well as pathophysiology of iTTP, suggest that both events may have contributed to this relapse. Previous publications reported imbalance of the vWF/ADAMTS13 axis in patients with COVID-192 and remarked that ADAMTS13 activity ranged from normal to significantly reduced.2 4 However, ADAMTS13 deficiency alone may not be sufficient to cause TTP.1 On the other hand, association between iTTP and infections is well described; it could be a result of inflammation-mediated increase in ADAMTS13 autoantibodies, complement activation and reduced cleavage of vWF by ADAMTS13.26 Hence, it is conceivable that COVID-19 infection could trigger iTTP. Similarly, there may be a causative link between vaccination and iTTP. Case reports of iTTP associated with influenza, pneumococcal and rabies vaccination were published previously.21 iTTP following different types of COVID-19 vaccines has also been reported.22–25 The time between vaccination and iTTP relapse was consistent at 5–7 days in most cases, whereas the time between vaccination and de novo iTTP was variable at 5–37 days (see online supplemental table 3). Ongoing surveillance for vaccine-associated complications, including iTTP, is warranted. Almost 500 million COVID-19 infections were reported globally to WHO and over 11 billion doses of COVID-19 vaccines were administered as of 13 April 2022.29 Our literature review identified 20 cases of de novo or relapsed iTTP in COVID-19-infected adult patients and 14 reports of iTTP after COVID-19 vaccination (see online supplemental tables). Considering the total number of infections and vaccinations, the reported number of COVID-19 infection or vaccine-associated iTTP cases remains very low. The medical and patient community should feel reassured about the safety of COVID-19 vaccine vis-à-vis risk of iTTP. COVID-19 infection appears to be a rare trigger for iTTP.

In conclusion, we presented a case of relapsed iTTP within 7 days of the first dose of Moderna mRNA COVID-19 vaccine with concurrent COVID-19 infection. The literature review identified a very low number of iTTP cases associated with either COVID-19 infection or vaccination, suggesting that neither COVID-19 infection nor vaccination represents a strong trigger for iTTP. Ongoing surveillance is warranted. Careful analysis of risks and benefits is required to decide on whether to proceed with anti-CD20 therapy in patients with iTTP and COVID-19 infection.

Patient’s perspective

Being in the ICU with COVID were the darkest days of my life, I feel lucky to have recovered.

Learning points

  • COVID-19 infection or vaccination-associated immune thrombotic thrombocytopenic purpura (iTTP) is very rare.

  • Post-vaccination monitoring for relapse may be warranted in patients with iTTP.

  • Risk of anti-CD20 therapy in patients with iTTP and COVID-19 infection is unclear.

Ethics statements

Patient consent for publication

References

Supplementary materials

  • Supplementary Data

    This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.

Footnotes

  • Twitter @BrandonTse3

  • Contributors FF collected data, conducted literature review and prepared the first draft of the manuscript. BT participated in literature review and writing of the manuscript. KP supervised the project and contributed to writing of the manuscript. All authors have read and approved the final manuscript.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Case reports provide a valuable learning resource for the scientific community and can indicate areas of interest for future research. They should not be used in isolation to guide treatment choices or public health policy.

  • Competing interests KP participated in industry-sponsored randomised controlled trials and received honoraria for speaking and consulting for Ablynx/Sanofi, Shire/Takeda.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.