key: cord-0872331-afd41l2o authors: Stebbings, Richard; Armour, Gillian; Pettis, Vivian; Goodman, Joanne title: AZD1222 (ChAdOx1 nCov-19): A Single-Dose biodistribution study in mice date: 2021-12-02 journal: Vaccine DOI: 10.1016/j.vaccine.2021.11.028 sha: cf94f70acf2587fe749601aaff75e667534793f7 doc_id: 872331 cord_uid: afd41l2o Biodistribution studies of adenovirus-based vaccines support their clinical development by evaluating their spread and persistence following in vivo administration. AZD1222 (ChAdox1 nCov-19) is a replication-deficient non-human adenovirus-vectored vaccine for coronavirus disease 2019. In this nonclinical study, the biodistribution of AZD1222 was assessed in mice for 29 days following intramuscular injection. Results show that AZD1222 was safe and well tolerated, with a spread that was largely confined to administration sites and the proximal sciatic nerve, with low levels observed in sites that are involved in rapid clearance of particulates by the reticuloendothelial system. Accordingly, levels of AZD1222 decreased from Day 2 to Day 29, indicating clearance. There were no quantifiable levels of AZD1222 in the blood, brain, spinal cord, and reproductive tissue, suggesting a lack of widespread or long-term distribution of AZD1222 vector DNA throughout the body following its administration. AZD1222 (ChAdOx1 nCov-19) is a replication-deficient simian adenovirus-vectored vaccine for coronavirus disease 2019 (COVID-19) that encodes the full-length severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein [1] . Therapeutic DNA vaccines such as this can induce cellular and humoral immune responses to specific antigens, modulate the immune system, and are very stable, conferring several advantages over conventional vaccines [2, 3] . Viral vectors are the most frequently used carriers to deliver and protect DNA [2] . Furthermore, nonhuman adenoviral vectors avoid the risk of pre-existing neutralizing antibodies to the vaccine vector itself that are commonly observed with, and may limit the efficacy of, equivalent human adenoviral vaccine vectors [4] . Biodistribution analyses of new therapeutic DNA vaccines evaluate the spread and persistence of the vector to target and nontarget tissues following direct administration in animals, and are routinely performed during product development. The biodistribution of DNA from different adenovector types has been evaluated in nonclinical studies, with results indicating that they are rapidly cleared from the body [5] . Furthermore, adenovectors have been shown to remain primarily at the site of administration in the muscle and subcutis, and variously trafficked to the liver, iliac lymph nodes, and spleen, but not to other distal organs, including remaining absent from the gonads. These seminal studies concluded that adenovirus vectors are safe and suitable for investigational human use, given intramuscularly, to prevent various infectious diseases [6] . Large phase 3 trials are designed to detect safety signals within prespecified timeframes, while pharmacovigilance of vaccine use in the real world may detect rare events that manifest only when tens of millions of people are vaccinated. Challenges lie in differentiating which safety signals from real-world use are related to the vaccine, and which have occurred coincidentally in the short risk interval after vaccine exposure. In very rare instances, a combination of thrombosis and thrombocytopenia has been reported following vaccination with COVID-19 vaccines, including AZD1222 [7] [8] [9] [10] . Independent safety reviews by regulatory authorities have, however, concluded that the balance of benefits and risks is firmly in favor of vaccination in adults of all age groups [11] . Biodistribution analyses may help evaluate the legitimacy of vaccine safety concerns by mapping the temporal dispersal of the vaccine following its administration. Because AZD1222 is replication-incompetent in human cells and is administered via intramuscular injection, upon initial infection of cells, the biodistribution or further infection and spread of the adenovirus is expected to be negligible and clinically insignifi- [12] . The objective of this study was, therefore, to determine the longitudinal and quantitative distribution of AZD1222 to multiple tissues (including the blood) following a single intramuscular injection in mice. Mice were chosen as they are considered immunologically relevant for vaccine toxicity testing, have previously been used to study HuCoV infection [13] and model COVID-19 [14] , and AZD1222 induces robust antibody and cellmediated immune responses in these animals [1] . Studies were conducted in an Organization for Economic Cooperation and Development (OECD) country and in accordance with OECD Test Guidelines and Principles of Good Laboratory Practice for nonclinical laboratory studies, complied with ARRIVE guidelines, and were conducted in accordance with the UK Animals (Scientific Procedures) Act, 1986. The study protocol was developed in accordance with United States Food and Drug Administration, European Medicines Agency, Japanese, and World Health Organization guidelines for assessing the potential toxicity of vaccines for infectious diseases. AZD1222 was the test agent. For control animals, AZD1222 vehicle was used. A total of 160 (80 male, 80 female) CD-1 mice aged 6-8 weeks obtained from Charles River Laboratories (Charles River UK Limited, Margate, Kent, UK) were randomly allocated (1:1) to vaccine or control groups. For each animal, 0.035 mL of vaccine or control was administered intramuscularly in the thigh muscle of each hindlimb (0.07 mL in total). For the test group, the dose exceeded the human dose on a mg/kg basis, and was the highest feasible dose that can be administered to mice via intramuscular injection, considering the limitations of vaccine concentration and the total volume that can be administered given animal welfare considerations [15] . Animals were thoroughly examined before dosing and were observed regularly throughout the day of dosing and throughout the study period for potential vaccine-related reactions. Following administration on Day 1, biodistribution of AZD1222 vector DNA (hereafter referred to as just AZD1222) to blood and feces was assessed on Days 2, 3, 5, and 9. Biodistribution of AZD1222 to tissues (administration sites, adrenal gland, axillary lymph node, bone marrow, brain, heart, inguinal lymph node, kidney, liver, lung, mammary gland, mesen-teric lymph node, ovaries, pancreas, sciatic nerve, spinal cord, spleen, testes, and thymus) was assessed on Days 2, 3, 9, or 29 following terminal anesthesia and complete necropsy examination. Terminal anesthesia was performed on five male and five female animals from each study group at each timepoint. Separate instruments were used to extract different tissues. Bone marrow was collected from the left femur. The concentration of AZD1222 relative to a DNA standard curve was determined by a validated method using quantitative polymerase chain reaction. Regression analysis was performed using Watson LIMS system (Version 7.4.2, Thermo-Fisher, Waltham, MA, USA). Sample results > limit of detection (LOD) (10 copies/reaction) were back-calculated to AZD1222 vector DNA concentration in copies/lg DNA. Samples between the LOD and lower limit of quantitation (LLOQ) of the assay (10 and 50 copies/reaction, respectively) were flagged in the corresponding tables as < LLOQ. AZD1222 was well-tolerated, and throughout the study there were no clinical observations, unscheduled deaths, changes in bodyweight, or changes in food consumption that were considered related to the administration of the vaccine. Furthermore, there were no quantifiable concentrations of AZD1222 in blood or feces samples collected from control or dosed animals, except for one feces sample from a dosed animal at Day 2 (1.03 Â 10 3 copies/lg DNA) Fig. 1 . In dosed animals, and across all timepoints, the highest levels of AZD1222 (>10 4 -10 7 copies/lg DNA) were observed in the two administration sites and the sciatic nerve (proximal to the injection site) with decreased levels for most animals at Day 9 and 29 (<10 4 copies/ lg DNA) Fig. 1 . Lower levels of AZD1222 (