{"id":30870,"date":"2022-12-16T16:05:19","date_gmt":"2022-12-16T17:05:19","guid":{"rendered":"https:\/\/peymantaeidi.net\/stem-cell\/?p=30870"},"modified":"2022-12-16T18:00:16","modified_gmt":"2022-12-16T18:00:16","slug":"she-hulk-an-incredible-case-of-transfusion-associated-graft-versus-host-disease","status":"publish","type":"post","link":"https:\/\/peymantaeidi.net\/stem-cell\/2022\/12\/16\/she-hulk-an-incredible-case-of-transfusion-associated-graft-versus-host-disease\/","title":{"rendered":"She-Hulk: an incredible case of transfusion associated graft versus host disease"},"content":{"rendered":"<div><img decoding=\"async\" src=\"https:\/\/peymantaeidi.net\/stem-cell\/wp-content\/uploads\/2022\/12\/8364.cover-source-scaled.jpg\" class=\"ff-og-image-inserted\" alt=\"image\" \/><\/div>\n<p><span class=\"highwire-journal-article-marker-start\"><\/span><\/p>\n<div class=\"contributors\">\n<ol class=\"contributor-list\" id=\"contrib-group-1\">\n<li class=\"last\" id=\"contrib-1\"><span class=\"name\">Neil A Barrett<\/span><span class=\"contrib-role\">, consultant paediatric haematologist<\/span><a id=\"xref-aff-1-1\" class=\"xref-aff\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#aff-1\">1<\/a><\/li>\n<\/ol>\n<ol class=\"affiliation-list\">\n<li class=\"aff\">\n<address><sup>1<\/sup>Children\u2019s Health Ireland\u2014Department of Haematology, Dublin, Ireland<\/address>\n<\/li>\n<\/ol>\n<ol class=\"corresp-list\">\n<li class=\"corresp\" id=\"corresp-1\"><span class=\"em-link\"><span class=\"em-addr\">neil.barrett{at}olchc.ie<\/span><\/span><\/li>\n<\/ol>\n<\/div>\n<div class=\"teaser\">\n<p id=\"p-1\"><strong>Neil Barrett<\/strong> discusses the unusual haematological implications of accidental transfusion from a close relative in the high profile case of the She-Hulk, barriers to future research, and the real heroes in this<\/p>\n<\/div>\n<p id=\"p-2\">Transfusion associated graft versus host disease (TaGVHD) is a rare complication of blood transfusion in which viable lymphocytes within a blood product engraft (survive and proliferate) in a recipient. This process results in an almost always fatal form of graft versus host disease,<a id=\"xref-ref-1-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-1\">1<\/a> with donor T cells attacking multiple organs, notably the skin, liver, gastrointestinal tract, and bone marrow.<\/p>\n<p id=\"p-3\">This paper analyses a high profile case of non-lethal TaGVHD due to inadvertent blood contamination of an open wound after a car accident.<a id=\"xref-ref-2-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-2\">2<\/a> While both donor and recipient survived the crash and contamination, the recipient was left with unexpected side effects, namely inheriting the ability of the donor to transform into an enormous green rage monster.<\/p>\n<p id=\"p-4\">The celebrity nature of this case means that the identities of both donor and recipient as well as the details of the incident are already in the public domain. The donor is Bruce Banner MD, PhD, PhD, PhD, PhD, PhD, PhD, PhD,<a id=\"xref-ref-3-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-3\">3<\/a> otherwise known as the strongest Avenger.<a id=\"xref-ref-4-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-4\">4<\/a> The recipient is Jennifer Walters, JD\u2014also known as She-Hulk<a id=\"xref-ref-2-2\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-2\">2<\/a> of high profile law firm Goodman, Lieber, Kurtzberg, and Holliway, the only legal firm in the world representing superhuman clients. Walters recently made headlines after a trademark dispute with Instagrammer Titania, and as such, no details of the case are confidential.<\/p>\n<p id=\"p-5\">This paper describes the risk factors for TaGVHD present in this case, discusses additional haematological phenomena that might be occurring, and suggests further research aims that might advance our understanding of transfusion medicine.<\/p>\n<div class=\"section cases\" id=\"sec-1\">\n<h2 class=\"\">Risk factors for TaGVHD present in the case<\/h2>\n<div id=\"sec-2\" class=\"subsection\">\n<h3>Shared genetic makeup<\/h3>\n<p id=\"p-6\">The donor has revealed that he and the recipient, his first cousin, share rare combination genetic factors that allow them to synthesise \u03b3 radiation.<a id=\"xref-ref-2-3\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-2\">2<\/a> They might also share HLA haplotypes. Among the risk factors for TaGVHD (<a id=\"xref-boxed-text-1-1\" class=\"xref-boxed-text\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#boxed-text-1\">box 1<\/a>), one is partial HLA similarity between the donor and host, because HLA similarity could give donor T cells an increased ability to avoid the host immune system and engraft.<a id=\"xref-ref-5-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-5\">5<\/a> For this reason (among many others), blood donations from one family member to another (eg, parent to child) are often strongly discouraged.<a id=\"xref-ref-6-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-6\">6<\/a><\/p>\n<div class=\"boxed-text\" id=\"boxed-text-1\"><span class=\"boxed-text-label\">Box 1<\/span> <\/p>\n<h3>Risk factors for TaGVHD and indications for blood product irradiation<\/h3>\n<div id=\"sec-3\" class=\"subsection\">\n<h4>Immunocompromised host<\/h4>\n<ul class=\"list-simple\" id=\"list-1\">\n<li id=\"list-item-1\">\n<p id=\"p-7\">Fetal recipients of intrauterine transfusion (IUT) or neonates who received previous IUT<\/p>\n<\/li>\n<li id=\"list-item-2\">\n<p id=\"p-8\">Patients with congenital T lymphocyte immune deficiency (not including HIV\/AIDS)<\/p>\n<\/li>\n<li id=\"list-item-3\">\n<p id=\"p-9\">Patients with history of Hodgkin\u2019s lymphoma<\/p>\n<\/li>\n<li id=\"list-item-4\">\n<p id=\"p-10\">Patients with previous T cell depleting treatment: anti-thymocyte globulin\u00a7, purine analogues, alemtuzimab\u00a7 <\/p>\n<\/li>\n<li id=\"list-item-5\">\n<p id=\"p-11\">Recipients of haematopoietic stem cell transplantation from time of conditioning*\u2020<\/p>\n<\/li>\n<\/ul>\n<\/div>\n<div id=\"sec-4\" class=\"subsection\">\n<h4>Degree of HLA matching between donor and recipient<\/h4>\n<\/div>\n<div id=\"sec-5\" class=\"subsection\">\n<h4>Product factors<\/h4>\n<\/div>\n<ul>\n<li class=\"fn\" id=\"fn-1\">\n<p id=\"p-16\">TaGVHD=transfusion associated graft versus host disease. <\/p>\n<\/li>\n<li class=\"fn\" id=\"fn-2\">\n<p id=\"p-17\">*For auto-transplantation, from eight days before collection to three months after transplantation; for allo-transplantation, from time of conditioning to at least six months after transplantation.<\/p>\n<\/li>\n<li class=\"fn\" id=\"fn-3\">\n<p id=\"p-18\">\u2020Potential instant conditioning in this case.<\/p>\n<\/li>\n<li class=\"fn\" id=\"fn-4\">\n<p id=\"p-19\">\u2021Present in this case.<\/p>\n<\/li>\n<li class=\"fn\" id=\"fn-5\">\n<p id=\"p-20\">\u00a7If not part of conditioning for solid organ transplantation or part of treatment of multiple sclerosis or vasculitis <\/p>\n<\/li>\n<\/ul>\n<p><a href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#xref-boxed-text-1-1\">RETURN TO TEXT<\/a><\/div>\n<p id=\"p-21\">It is noted that in extremis (noted as an adjective, and not to be confused with EXTREMIS bioelectric nanotechnology developed by Maya Hansan and Aldrich Killian), alternate versions of Dr Banner rampaging around the multiverse, with total disregard to best transfusion practice, carried out a direct donation<a id=\"xref-ref-7-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-7\">7<\/a> of his own blood to prevent Ms Walters exsanguinating from a similar accident.<\/p>\n<\/div>\n<div id=\"sec-6\" class=\"subsection\">\n<h3>Instant conditioning<\/h3>\n<p id=\"p-22\">Patients with immunocompromising conditions are also at higher risk for TaGVHD, for example, those who have undergone regimens for stem cell transplantation conditioning such as total body irradiation. In this case, the recipient received a so-called lethal dose of \u03b3 radiation,<a id=\"xref-ref-2-4\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-2\">2<\/a> which could have weakened her endogenous T lymphocyte response enough to lead to engraftment\u2014in effect, a form of instantaneous transplantation conditioning.<\/p>\n<\/div>\n<div id=\"sec-7\" class=\"subsection\">\n<h3>Whole non-leucodepleted blood<\/h3>\n<p id=\"p-23\">In the present case, whole, unfiltered (non-leucodepleted) blood without exogenous irradiation was introduced from the donor into the recipient. In the UK, universal pre-storage leucodepletion of blood products was introduced in 1999 with the primary intention to reduce transmission risk of variant Creutzfeldt-Jakob disease in the blood supply. However, several other benefits have been observed,<a id=\"xref-ref-8-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-8\">8<\/a> including a reduced risk of other infections through transfusion (notably cytomegalovirus<a id=\"xref-ref-9-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-9\">9<\/a>) and lower occurrence of TaGVHD. With widespread pre-storage leucodepletion, no cases of TaGVHD involving leucodepleted blood<a id=\"xref-ref-10-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-10\">10<\/a> in the UK have been reported in the annual haemovigilance SHOT (serious hazards of transfusion) reports<a id=\"xref-ref-11-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-11\">11<\/a> in more than 20 years. However, the definition of adequate leucoreduction depends on statistical sampling of a small proportion of cellular products. This process might fail to achieve desired levels of depletion in all patients, and certainly TaGVHD continues to be reported internationally in the era of leucodepletion. While filtration is generally highly efficient,<a id=\"xref-ref-12-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-12\">12<\/a> concerns could arise in the setting of Hulk lymphocytes that might be able to \u201csmash\u201d through filters. <\/p>\n<\/div>\n<\/div>\n<div class=\"section other1\" id=\"sec-8\">\n<h2 class=\"\">Irradiation<\/h2>\n<p id=\"p-24\">In the presence of risk factors for TaGVHD (<a id=\"xref-boxed-text-1-2\" class=\"xref-boxed-text\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#boxed-text-1\">box 1<\/a>), irradiation is used as additional step to eliminate engraftment potential of any residual T lymphocytes that might be present after leucodepletion. The 2020 guideline from the British Committee for Standards in Haematology for use of irradiated blood components recommends that irradiation delivers at least 25 Gy of x ray or \u03b3 radiation, with strict control of dose and distribution within the product.<a id=\"xref-ref-13-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-13\">13<\/a><\/p>\n<p id=\"p-25\">Standard dose irradiation of blood component from a Hulk (both made of \u03b3<a id=\"xref-ref-14-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-14\">14<\/a> and purportedly resistant to \u03b3 radiation), even if donated while in human form, might not be efficacious. <\/p>\n<p id=\"p-26\">While Dr Banner has never specifically mentioned an immunity to the effects of x rays, their lower energy relative to the highest energy \u03b3 rays could be described as \u201cpuny\u201d (to paraphrase Dr Banner) and might therefore be insufficient for irradiating Hulk blood component. <\/p>\n<p id=\"p-27\">The \u201cgamma\u201d produced endogenously within Dr Banner apparently does not suppress his T cells to the point that he experiences recurrent infections. However, \u201cgamma\u201d produced in Ms Walters\u2019 post-transfusion blood could be modulating donor T cells, thereby preventing fatal effects of graft versus host disease. Her ability to produce \u201cgamma\u201d is different (in a better way)<a id=\"xref-ref-2-5\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-2\">2<\/a> from her cousin\u2019s and could provide engrafted cells with \u201cjust the right amount of rage.\u201d<\/p>\n<p id=\"p-28\">Hulks can have prolonged side effects from very high levels of \u03b3 radiation, including after exposure to infinity stones.<a id=\"xref-ref-14-2\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-14\">14<\/a> However, because most blood processing facilities lack access to infinity gauntlets, achieving this level of \u03b3 dosage is impossible for most blood centres.<\/p>\n<\/div>\n<div class=\"section discussion\" id=\"sec-9\">\n<h2 class=\"\">Discussion<\/h2>\n<p id=\"p-29\">In this incredible case of non-lethal TaGVHD, whole blood transfusion from donor to recipient with multiple risk factors for TaGVHD seems to have merely transferred superhuman abilities. Several extraordinary factors could have safeguarded against disaster in this accidental transfusion. While wildly speculative, the endogenous \u03b3 production unique to Ms Walters\u2019 genetic makeup could have been key in the modulation of engrafted cell activity specifically preventing fatal TaGVHD; therefore, the outcome of this accidental transfusion might not be readily reproducible.<\/p>\n<p id=\"p-30\">While attempts have since been made to gain access to samples from Ms Walters, replication studies are unlikely. Dr Banner has strongly refused any attempts to replicate the findings, going so far as to destroy all known samples of Ms Walters\u2019 blood (it is considered inadvisable to make him angry).<a id=\"xref-ref-2-6\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-2\">2<\/a> Furthermore, ethics committees are unlikely to approve further research under the rules of the Helsinki declaration,<a id=\"xref-ref-15-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-15\">15<\/a> or indeed under the Sokovia accords (although New York based attorney Matt Murdock confirmed during a recent public court proceeding that the Sokovia accords have been repealed).<\/p>\n<p id=\"p-31\">While HLA disparities between Hulk blood and human recipients could reduce the risk of TaGVHD, transfusion of blood from Hulks remains highly inadvisable on safety grounds, even with leucodepletion and irradiation. Given unpredictable outcomes, any history of so-called Hulk-ing out or turning into an enormous green rage monster should be added to the exclusion criteria for blood donation in pre-donation screening questionnaires.<a id=\"xref-ref-16-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-16\">16<\/a><a id=\"xref-ref-17-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-17\">17<\/a><\/p>\n<p id=\"p-32\">Several other manifestations of TaGVHD in this case warrant further discussion. Firstly, the verdant hue of the recipient raises several questions based on our current, nascent understanding of Hulk physiology and knowledge of graft versus host disease. In particular, why a green colour rather than red or yellow? <\/p>\n<p id=\"p-33\">In TaGVHD, infiltration of the of the skin by engrafted donor T lymphocytes typically produces a diffuse, erythrodermic (red) rash. Red Hulks have been described in case reports,<a id=\"xref-ref-18-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-18\">18<\/a> with near global skin effects characterised by intense heat emission, consistent with acute inflammation or indeed hyperfebrile reactions. Alternatively, graft versus host disease of the liver could cause hepatic failure, giving rise to jaundice. Yellow Hulks have also been described in preprints,<a id=\"xref-ref-19-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-19\">19<\/a> and intense pruritus might of course be enraging. Even more notably, advanced graft versus host disease of the liver could produce a prolonged conjugated hyperbilirubinemia and a more classical Hulk green skin as cutaneous bilirubin is oxidised to biliverdin.<a id=\"xref-ref-20-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-20\">20<\/a> In the present case, it is not clear whether the discolouration of Walters\u2019 skin results from a genetic trait specific to her family or an attribute of the donor. Given the apparently high tolerance of alcohol observed in Hulks,<a id=\"xref-ref-2-7\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-2\">2<\/a> liver disease is unlikely to be the mechanism.<\/p>\n<p id=\"p-34\">Secondly, Ms Walters now also experiences reversible, stress induced muscular hypertrophy with unclear underlying physiological mechanism. One possibility is that the inadvertently transfused peripheral blood contained cells with myogenic potential. Cells in the peripheral blood expressing the surface marker CD133 have been shown to have the ability to form muscular satellite cells and myofibres.<a id=\"xref-ref-21-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-21\">21<\/a> Since physiological<a id=\"xref-ref-22-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-22\">22<\/a> and even psychological stress<a id=\"xref-ref-23-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-23\">23<\/a> can cause mobilisation of stem cells of various potentials into peripheral blood, this mechanism could underlie both the enrichment of the transfused blood with stem cells (at the time of an accident caused by unexpected alien visitation) and the subsequent ability of the recipient to transform when she allows her stress to manifest (although in an exceptionally controlled manner).<\/p>\n<p id=\"p-35\">Finally, there is one somewhat related report<a id=\"xref-ref-24-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-24\">24<\/a> of a failed attempt to transfer superhuman capabilities via bone marrow transplantation. Owing to the reclusive donor\u2019s history of orthopaedic surgery, harvesting bone marrow from his bone claws\u2014a non-traditional harvest site\u2014would require adamantium (or vibranium) collection needles, or, indeed, a gigantic adamantium samurai exosuit and remains purely theoretical.<\/p>\n<\/div>\n<div class=\"section conclusions\" id=\"sec-10\">\n<h2 class=\"\">Conclusion<\/h2>\n<p id=\"p-36\">While superheroes as blood and bone marrow donors capture the imagination, the safety of engaging superpowered individuals as donors is far from established. However, it is hoped that this case encourages normal humans to donate blood\u2014allowing them to become the real heroes. The current campaign by UK NHS Blood and Transplant and the Wakandan government, \u201cNot Family, but Blood\u201d (#inourblood),<a id=\"xref-ref-25-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-25\">25<\/a> highlights the urgent need for blood donors of Black African or Black Caribbean heritage, owing to the increased diversity of red blood cell antigens and the increased incidence of blood disorders such as sickle cell disease<a id=\"xref-ref-26-1\" class=\"xref-bibr\" href=\"https:\/\/www.bmj.com\/content\/379\/bmj-2022-074148#ref-26\">26<\/a> within this population group. Real heroes rising from superpowered tales would be truly incredible.<\/p>\n<\/div>\n<div class=\"section fn-group\" id=\"fn-group-1\">\n<h2>Footnotes<\/h2>\n<ul>\n<li class=\"fn-conflict\" id=\"fn-6\">\n<p id=\"p-37\">Competing interests: I have read and understood BMJ policy on declaration of interests and declare the following interests: none.<\/p>\n<\/li>\n<li class=\"fn-other\" id=\"fn-7\">\n<p id=\"p-38\">Provenance and peer review: Commissioned; externally peer reviewed.<\/p>\n<\/li>\n<\/ul>\n<\/div>\n<p><span class=\"highwire-journal-article-marker-end\"><\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Neil A Barrett, consultant paediatric haematologist1 1Children\u2019s Health Ireland\u2014Department of Haematology, Dublin, Ireland neil.barrett{at}olchc.ie Neil<\/p>\n","protected":false},"author":1,"featured_media":30872,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"_links":{"self":[{"href":"https:\/\/peymantaeidi.net\/stem-cell\/wp-json\/wp\/v2\/posts\/30870"}],"collection":[{"href":"https:\/\/peymantaeidi.net\/stem-cell\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/peymantaeidi.net\/stem-cell\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/peymantaeidi.net\/stem-cell\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/peymantaeidi.net\/stem-cell\/wp-json\/wp\/v2\/comments?post=30870"}],"version-history":[{"count":2,"href":"https:\/\/peymantaeidi.net\/stem-cell\/wp-json\/wp\/v2\/posts\/30870\/revisions"}],"predecessor-version":[{"id":30873,"href":"https:\/\/peymantaeidi.net\/stem-cell\/wp-json\/wp\/v2\/posts\/30870\/revisions\/30873"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/peymantaeidi.net\/stem-cell\/wp-json\/wp\/v2\/media\/30872"}],"wp:attachment":[{"href":"https:\/\/peymantaeidi.net\/stem-cell\/wp-json\/wp\/v2\/media?parent=30870"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/peymantaeidi.net\/stem-cell\/wp-json\/wp\/v2\/categories?post=30870"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/peymantaeidi.net\/stem-cell\/wp-json\/wp\/v2\/tags?post=30870"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}