The use of high-dose intravenous immune globulin (IVIG) plus anticoagulation is recommended for the treatment of vaccine-induced immune thrombotic thrombocytopenia (VITT), a rare side effect of adenoviral vector vaccines against coronavirus disease 2019 (Covid-19). We describe the response to IVIG therapy in three of the first patients in whom VITT was identified in Canada after the receipt of the ChAdOx1 nCoV-19 vaccine. The patients were between the ages of 63 and 72 years; one was female. At the time of this report, Canada had restricted the use of the ChAdOx1 nCoV-19 vaccine to persons who were 55 years of age or older on the basis of reports that VITT had occurred primarily in younger persons. Two of the patients in our study presented with limb-artery thrombosis; the third had cerebral venous and arterial thrombosis. Variable patterns of serum-induced platelet activation were observed in response to heparin and platelet factor 4 (PF4), indicating the heterogeneity of the manifestations of VITT in serum. After the initiation of IVIG, reduced antibody-induced platelet activation in serum was seen in all three patients. (Funded by the Canadian Institutes of Health Research.)
Recently, vaccination with adenoviral vector vaccines against coronavirus disease 2019 (Covid-19) has been implicated in a rare prothrombotic disorder that has been termed vaccine-induced immune thrombotic thrombocytopenia (VITT).1-5 Most patients in whom VITT has been diagnosed have been between the ages of 20 and 55 years and have presented with unusual thromboses, such as cerebral venous sinus thrombosis and splanchnic-vein thrombosis.1-5 The pathogenesis involves the production of IgG antibodies that recognize platelet factor 4 (PF4) and that strongly activate platelets through their Fc¦ÃIIa receptors, leading to a decrease in the number of platelets (platelet consumption) and activation of coagulation.1,3 The disorder strongly mimics autoimmune heparin-induced thrombocytopenia (HIT)6-8 on the basis of both clinical and serologic evidence, even though patients with VITT usually have not received heparin.
High-dose intravenous immune globulin (IVIG) competitively inhibits the interaction of VITT antibodies with the platelet Fc¦ÃIIa receptors, thus reducing platelet activation ¡ª a result that may be an important treatment consideration. Since minimal data exist for treating patients with VITT, the recommended use of IVIG is based primarily on an analogy with treatment of autoimmune HIT, in which the administration of IVIG rapidly increases the platelet count and reduces hypercoagulability.9-11 Our report documents the inhibition of serum-induced platelet activation after treatment with IVIG in three patients in whom VITT was diagnosed between March 31 and April 13, 2021. Our study also shows how the serotonin-release assay ¡ª the most common laboratory test of platelet activation that is performed to detect HIT in North American reference laboratories ¡ª can be adapted to detect VITT antibodies.
Patient 1 was a 72-year-old woman with an unremarkable medical history who reported having an onset of left limb pain and claudication 7 days after vaccination with ChAdOx1 nCoV-19 (Covishield, an AstraZeneca vaccine licensed for production by the Serum Institute of India). Her symptoms progressed, and she was admitted to the hospital 8 days after symptom onset. Imaging showed a suprarenal aortic thrombus, with occlusion of the left superficial and deep femoral arteries, plus partial thromboses of the celiac and right peroneal arteries. At that time, a disorder resembling heparin-induced thrombocytopenia was not suspected, so unfractionated heparin was started; 3 days later, the patient underwent surgical embolectomy. By that time, VITT was suspected, and argatroban was initiated. Since there was no improvement in the platelet count during a 5-day period, high-dose IVIG was administered. The patient¡¯s platelet count increased, and she was discharged home while receiving oral apixaban.
Patient 2 was a 63-year-old man without cardiovascular risk factors or a history of thrombosis who reported having cramping in his left leg beginning 18 days after vaccination. Four days later, acute dyspnea developed. The following day, his left leg became painful and cold. He presented to the emergency department (24 days after vaccination), at which time computed tomographic angiography showed acute arterial thrombosis in the left leg, plus extensive pulmonary embolism. He received tinzaparin (low-molecular-weight heparin) and underwent surgical embolectomy. Lower-limb ultrasonography revealed nonocclusive right popliteal deep-vein thrombosis. Suspicion of VITT prompted a switch from heparin to fondaparinux and the administration of IVIG. Although no new thromboses occurred after IVIG treatment, residual distal lower-limb thrombosis resulted in distal foot ischemic necrosis, and at the time of this report, the patient was awaiting amputation.
Patient 3 was a 69-year-old man with non¨Cinsulin-dependent diabetes mellitus, hypertension, obstructive sleep apnea, recently diagnosed prostate cancer (not yet staged), and no history of thrombosis; he had a history of heparin exposure 9 months earlier during transcatheter aortic-valve replacement, which was followed by the administration of aspirin (81 mg) daily. Twelve days after vaccination, he reported having headache and confusion and was admitted to the hospital with progressive left-sided weakness. The diagnosis of VITT was made on hospital day 3 when further left-sided weakness became evident; right middle cerebral-artery stroke with hemorrhagic transformation was identified. Additional thromboses were documented in the right internal carotid artery, right cerebral transverse and sigmoid sinuses, right internal jugular vein, hepatic vein, and distal lower-limb vein; pulmonary embolism was also found. He was treated with fondaparinux and IVIG. No new clinically evident thromboses were subsequently observed, although the patient continued to have hemiplegia.
A recurrence of thrombocytopenia led to the administration of additional IVIG, which was followed by a transient improvement in the platelet count, along with a switch to rivaroxaban owing to a concern about VITT antibody cross-reactivity with fondaparinux; however, this cross-reactivity was ruled out by laboratory testing. Subsequently, the patient underwent therapeutic plasma exchange with the use of solvent detergent plasma as replacement fluid, which was administered in 13 exchanges from day 47 to day 62 after vaccination. The patient had subsequent gradual improvement in his platelet count, which reached a normal level of 158,000 per cubic millimeter on day 62.
Written informed consent for publication of their data was obtained from all three patients or their substitute decision makers. Serum was obtained both before and after the administration of IVIG to identify any changes in platelet-activating reactivity (ex vivo studies). We used a commercial immunoassay to detect antibodies against PF4¨Cpolyanion complexes (LIFECODES PF4 IgG/IgA/IgM enzyme-linked immunosorbent assay [ELISA], Immucor), according to the manufacturer¡¯s instructions. We also performed a serotonin-release assay, in which the patient¡¯s serum was incubated with donor platelets containing radioactive 14C serotonin and various levels of heparin. On this assay, when antibody that is present in the serum binds and activates donor platelets, it releases radiolabeled serotonin from the platelet granules. Thus, a higher percentage of serotonin release indicates greater platelet activation.12 However, we also used an assay that included a modification in which increasing doses of PF4 were added to the serum rather than heparin.13 We performed other assays with high levels of unfractionated heparin (100 U per milliliter), Fc receptor¨Cblocking monoclonal antibody (IV.3) (5 ¦Ìg per milliliter), and IVIG (Gammagard Liquid, Shire Pharma) (10 mg per milliliter). Weak reactivity was defined as a serotonin release of 20% to 49.9%, and strong reactivity as a release of more than 80%.
Platelet Changes after IVIG
Figure 1 shows serial platelet counts for the three patients in relation to treatment with anticoagulant and IVIG. Data regarding the patients¡¯ height, weight, and dosing considerations for IVIG administration (according to the Ontario dose calculator14) are provided in the Figure 1 legend.
In Patient 1, the platelet count rose from 39,000 to 77,000 per cubic millimeter during treatment with intravenous heparin, which was stopped before surgery. The platelet count did not change postoperatively during the 5-day administration of argatroban. However, after the administration of IVIG, the platelet count rose from 74,000 to 114,000 per cubic millimeter during a 2-day period, at which time the patient was discharged while receiving oral apixaban. At a follow-up visit 9 days later, the platelet count had normalized at 166,000 per cubic millimeter. Although mild thrombocytopenia recurred during the next 3 weeks, the d-dimer levels normalized.
In Patient 2, the platelet count initially rose from 36,000 to 77,000 per cubic millimeter after the administration of intravenous heparin. Subsequently, the platelet count fell, and heparin was switched to fondaparinux. After treatment with IVIG, the platelet count rose from 27,000 to 124,000 per cubic millimeter during a 3-day period; 7 days after the initiation of IVIG, the platelet count was 640,000 per cubic millimeter.
In Patient 3, no initial heparin was given. After VITT was diagnosed, IVIG and fondaparinux were administered, which resulted in an increase in the platelet count from 35,000 to 125,000 per cubic millimeter during a 3-day period, followed by a decrease to 106,000 per cubic millimeter and an increase in the d-dimer level; after a third dose of IVIG (as shown in the fourth blood sample), the platelet count rose to 165,000 per cubic millimeter, and the d-dimer level fell once again.
None of the three patients had clinical evidence of new or progressive thrombosis after IVIG treatment.
Two of the three patients (Patients 2 and 3) had evidence of disseminated intravascular coagulation, including elevated d-dimer levels (>10 and >20 mg per liter, respectively [reference range, <0.50]), low-normal fibrinogen levels (140 and 200 mg per deciliter, respectively [reference range, 160 to 420]), and a mildly increased international normalized ratio (peak, 1.3 and 1.4, respectively [reference range, <1.2]). These results met the criteria for overt disseminated intravascular coagulation.15 After treatment with IVIG, the two patients had a reduction in serial d-dimer levels and an increase in serial fibrinogen levels, findings that were consistent with decreased hypercoagulability.
Platelet Immunologic Analyses
All three patients tested strongly positive for antibodies against PF4¨Cpolyanion complexes on ELISA (Table 1). No consistent reduction in ELISA reactivity was seen after treatment with IVIG, which indicated that IVIG did not inhibit VITT antibody binding to PF4. Patient 2 tested negative on a latex-based immunoturbidimetric assay (HemosIL HIT-Ab(PF4-H), Instrumentation Laboratory), a local rapid-screening test for HIT antibodies. According to a recent report,4 this screening test has shown negative results for VITT antibodies.
Serum obtained before IVIG administration (baseline) in the three patients showed three different reaction patterns on the serotonin-release assay, the standard platelet-activation assay for HIT. Patient 1 tested weakly positive for HIT, with serum producing 19% serotonin release with heparin at a concentration of 0 U per milliliter, 41% at 0.1 U per milliliter, 23% at 0.3 U per milliliter, and 0% at 100 U per milliliter (Figure 2A). (On this assay, a positive result is a release of >20% with heparin at a concentration of 0.1 U per milliliter or at a concentration of 0.3 U per milliliter that is inhibited at 100 U per milliliter.) Testing of serum from Patient 2 showed an atypical result, with 35% serotonin release observed in the absence of heparin that was inhibited to less than 5% with the addition of heparin at a concentration of 0.1 U per milliliter and 0.3 U per milliliter. Testing of serum from Patient 3 also showed an atypical result, with serotonin release of 78% with heparin at a concentration of 0 U per milliliter and 72% at 0.1 U per milliliter. For all three patients, serum-induced serotonin release was not observed after one or two doses of IVIG.
In Patients 1 and 2, the addition of PF4 (10 ¦Ìg per milliliter) to serum obtained at baseline showed strong (>80%) serotonin release (Figure 2B). No effect of PF4 was seen in the baseline serum from Patient 3, which showed a 78% serotonin release in the absence of PF4. In all three patients, serum that was obtained after IVIG treatment showed a reduction in reactivity in the presence of PF4; these reductions ranged from marked (in Patient 3) to minor (in Patient 2). Patient 2, whose serum showed the least reduction in serotonin release in the presence of PF4 after IVIG administration, had the greatest increase in the platelet count (from 27,000 to 640,000 per cubic millimeter during a 7-day period).
The use of high-dose IVIG to treat thrombosis is unusual, especially considering that thrombotic events have been well documented after IVIG administration in patients with immune thrombocytopenic purpura, a hemorrhagic disorder.16,17 However, in the case of patients with autoimmune HIT9-11 and in our three study patients with VITT, the inhibition of serum-induced platelet-activating properties by IVIG was associated with increased platelet counts.
These findings probably reflect in vivo inhibition of antibody-induced platelet activation and reduced hypercoagulability, as shown by an increase in fibrinogen levels and a decrease in d-dimer levels in Patients 2 and 3. Increasing the platelet count is especially important when patients have severe thrombocytopenia and multiple unusual thromboses that require therapeutic-dose anticoagulation, especially in the context of hemorrhagic transformation after cerebral infarction. Moreover, antibodies that have been implicated in HIT also activate monocytes18 and neutrophils19 through membrane Fc¦Ã receptors. Since patients with VITT can have severe thrombocytopenia that potentially lasts for several weeks, early administration of IVIG may be an important adjunct therapy to anticoagulation for the management of VITT. Currently, several VITT treatment guidelines recommend up-front administration of high-dose IVIG when VITT is strongly suspected and thrombosis is present.20-22 The dosing recommendation of 1 g per kilogram of body weight20-22 on two consecutive days (i.e., a total of 2 g per kilogram) can be ambiguous, since the applicable body weight can range from ¡°ideal¡± to ¡°actual¡± weight or an intermediate value called ¡°dosing¡± weight.14 We suggest the use of dosing weight at the very least and preferably the actual body weight in making these calculations,20,22 given the dose-dependent effects of IVIG in decreasing antibody-induced platelet activation.9,23
Our study also shows how the platelet-activation test used in North American reference laboratories ¡ª the serotonin-release assay ¡ª can be adapted to detect VITT antibodies by including a reaction well for PF4. Recently, Greinacher and colleagues1 found that supplementation of PF4 (10 ¦Ìg per milliliter) was helpful in diagnosing VITT with the use of a washed-platelet activation test based on visual detection of platelet aggregation. We found that the reactivity patterns of the serum obtained from our study patients with VITT were heterogeneous, since two samples tested positive (one weakly) on the conventional test for HIT, although the reaction pattern in serum obtained from Patient 3 was atypical. In Patients 1 and 2, who had weak and negative results, respectively, on the conventional test for heparin-dependent antibodies, the addition of PF4 resulted in strong serotonin release. Thus, we suggest that testing for HIT and VITT antibodies can be readily accomplished by performing the standard platelet-activation assay at the usual conditions, with the addition of PF4 (¡Ý10 ¦Ìg per milliliter) without heparin. We also recommend testing at 0 U per milliliter as a buffer control, since serum-induced serotonin release in the absence of heparin is a feature of autoimmune HIT.6,7 Our observations support the recommendation to test for VITT antibodies in serum before IVIG administration to avoid false negative results on the serotonin-release assay.24 In contrast, ELISA reactivity was not inhibited by IVIG treatment, as shown in Table 1 and as reported in patients with HIT.9,23
In our study, we describe three of the first patients in Canada in whom VITT was diagnosed after ChAdOx1 nCoV-19 vaccination. All three patients received doses of vaccine that were produced by the Serum Institute of India, which at the time of this study had supplied approximately two thirds of the ChAdOx1 nCoV-19 doses administered in Canada.25 After the initial cases of VITT were reported in Europe (beginning in late March 2021), the rollout of the AstraZeneca vaccine program in Canada was restricted to persons who were 55 years of age or older. This restriction accounted for the older ages of our three patients (72, 63, and 69 years of age). Of note, all three patients had one or more arterial thrombotic events. In addition, two patients had venous thrombosis. Of the 41 patients with VITT who had been described at the time of this report, arterial thrombosis had been diagnosed in only 5.1-5 However, the patients who have been described in other studies were mostly younger than those in our report. We suspect that older persons with VITT may be more likely to present with arterial thrombotic events.
Funding and Disclosures
Supported by a grant (CIHR 452655, to Dr. Nazy) from the
Disclosure forms provided by the authors are available with the full text of this article at NEJM.org.
Editor¡¯s note: After the submission of this manuscript, an independent group of authors submitted a summary of the case of Patient 2 reported here to the Canadian Medical Association Journal, and that report has been published (CMAJ 2021 June 14;193:E906-910).
This article was published on June 9, 2021, and last updated on June 21, 2021, at NEJM.org.
We thank Jane C. Moore, B.Sc., for technical assistance; Jo-Ann I. Sheppard, B.Sc., for preparing earlier versions of the figures; Genevieve Huynh-Trudeau, M.D., Renaud Allen-Lefebvre, M.D., and the entire team involved in the care of Patient 1; and Elizabeth A. MacKay, M.D., Leslie Skeith, M.D., Paul F. Petrasek, M.D., Melissa Jones, M.D., Annie Boisvert, M.D., and the entire teams involved in the care of Patients 2 and 3.
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Citing Article (1)
|Patient No.||ELISA Results|
|Before IVIG||After First IVIG Dose||After Second IVIG Dose||After Third IVIG Dose||After Fourth IVIG Dose|
Results are shown in optical density (OD) units on enzyme-linked immunosorbent assay (ELISA) for IgG, IgA, and IgM antibodies against platelet factor 4 (PF4)¨Cpolyanion complexes (reference value, 0.40 OD units) before and after the administration of intravenous immune globulin (IVIG) in the three study patients. No consistent reduction in ELISA reactivity was seen after treatment with IVIG, which indicates that IVIG did not inhibit VITT antibody binding to PF4. The addition of a high level of heparin (100 U per milliliter) inhibited reactivity by more than 90% in all 12 samples tested (not shown in the table). NA denotes not applicable.
- Clinical and Laboratory Data for the Three Study Patients with VITT.
- ELISA Reactivity before and after Treatment with IVIG.*
- Results of Platelet-Activation Assays.