Humoral response and breakthrough infections with SARS-CoV-2 B.1.617.2 variant in vaccinated maintenance hemodialysis patients

被引:18
|
作者
Wand, Ori [1 ,2 ]
Nacasch, Naomi [2 ,3 ]
Fadeela, Ayman [4 ]
Shashar, Moshe [5 ,6 ]
Grupper, Ayelet [2 ,7 ]
Benchetrit, Sydney [2 ,3 ]
Erez, Daniel [2 ,8 ]
Shitrit, Pnina [2 ,9 ]
Cohen-Hagai, Keren [2 ,3 ]
机构
[1] Meir Med Ctr, Dept Pulmonol, Kefar Sava, Israel
[2] Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel
[3] Meir Med Ctr, Dept Nephrol & Hypertens, Kefar Sava, Israel
[4] Meir Med Ctr, Corona & Resp Viruses Lab, Kefar Sava, Israel
[5] Laniado Hosp, Dept Nephrol & Hypertens, Netanya, Israel
[6] Technion, Ruth & Bruce Rappaport Fac Med, Haifa, Israel
[7] Tel Aviv Sourasky Med Ctr Tel Aviv, Dept Nephrol & Hypertens, Tel Aviv, Israel
[8] Meir Med Ctr, Dept Internal Med, Kefar Sava, Israel
[9] Meir Med Ctr, Infect Control Unit, Kefar Sava, Israel
关键词
Breakthrough COVID-19 infection; SARS-CoV-2; variant; BNT162b2; vaccine; Maintenance hemodialysis;
D O I
10.1007/s40620-022-01245-9
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Introduction Breakthrough COVID-19 may occur in vaccinated people, and may result from declining vaccine effectiveness or highly transmittable SARS-CoV-2 variants, such as the B.167.2 (delta) variant. We investigated risk factors and outcomes for infection with the delta variant among vaccinated hemodialysis patients. Methods Patients on maintenance hemodialysis who received two doses of the BNT162b2 (Pfizer-BioNTech) vaccine were analysed according to having developed COVID-19 (study group) or not (control group), in a retrospective, observational, comparative study. We compared risk-factors for developing breakthrough COVID-19 and assessed clinical outcomes, including 30-day mortality rates. Results Twenty-four cases of breakthrough SARS-CoV-2 infection were compared to 91 controls without infection. Breakthrough infection was associated with chronic immunosuppressive treatment, hematological malignancies, and low antibody levels against SARS-CoV-2 spike protein. All COVID-19 cases occurred at least 5 months after vaccination, and most were caused by the B.1.617.2 variant (at least 23/24 cases). COVID-19 was categorized as severe or critical disease in 11/24 patients (46%), and 54% required hospitalization and COVID-19-directed treatment. The source of infection was nosocomial in 6/24 cases (25%), and healthcare-related in 3/24 (12.5%). Mortality rate was 21%. Overall mortality was significantly higher in patients who developed COVID-19 than in controls (odds ratio for all-cause mortality 7.6, 95% CI 1.4-41, p = 0.002). Conclusions Breakthrough COVID-19 with the B.1.617.2 variant can occur in vaccinated hemodialysis patients and is associated with immunosuppression and weaker humoral response to vaccination. Infections may be nosocomial and result in significant morbidity and mortality. [GRAPHICS] .
引用
收藏
页码:1479 / 1487
页数:9
相关论文
共 50 条
  • [21] Clinical and Immunological Features of SARS-CoV-2 Breakthrough Infections in Vaccinated Individuals Requiring Hospitalization
    Lamacchia, Giulia
    Mazzoni, Alessio
    Spinicci, Michele
    Vanni, Anna
    Salvati, Lorenzo
    Peruzzi, Benedetta
    Bencini, Sara
    Capone, Manuela
    Carnasciali, Alberto
    Farahvachi, Parham
    Rocca, Arianna
    Kiros, Seble Tekle
    Graziani, Lucia
    Zammarchi, Lorenzo
    Mencarini, Jessica
    Colao, Maria Grazia
    Caporale, Roberto
    Liotta, Francesco
    Cosmi, Lorenzo
    Rossolini, Gian Maria
    Bartoloni, Alessandro
    Maggi, Laura
    Annunziato, Francesco
    JOURNAL OF CLINICAL IMMUNOLOGY, 2022, 42 (07) : 1379 - 1391
  • [22] Immunosuppressive treatments selectively affect the humoral and cellular response to SARS-CoV-2 in vaccinated patients with vasculitis
    Monti, Sara
    Fornara, Chiara
    Delvino, Paolo
    Bartoletti, Alice
    Bergami, Federica
    Comolli, Giuditta
    Sammartino, Jose Camilla
    Biglia, Alessandro
    Cassione, Emanuele Bozzalla
    Cassaniti, Irene
    Baldanti, Fausto
    Lilleri, Daniele
    Montecucco, Carlomaurizio
    RHEUMATOLOGY, 2023, 62 (02) : 726 - 734
  • [23] Trends and Correlates of Breakthrough Infections With SARS-CoV-2
    Yamal, Jose-Miguel
    Appana, Savitri
    Wang, Mengxi
    Leon-Novelo, Luis
    Bakota, Eric
    Ye, Yuanqing
    Sharma, Shreela
    Morrison, Alanna C.
    Marko, Dritana
    Linder, Stephen H.
    Rector, Alison
    Jetelina, Katelyn K.
    Boerwinkle, Eric
    de Oliveira Otto, Marcia
    FRONTIERS IN PUBLIC HEALTH, 2022, 10
  • [24] Superior humoral immunity in vaccinated SARS-CoV-2 convalescence as compared to SARS-COV-2 infection or vaccination
    Paniskaki, Krystallenia
    Konik, Margarethe J.
    Anft, Moritz
    Meister, Toni L.
    Marheinecke, Corinna
    Pfaender, Stephanie
    Jaeger, Jasmin
    Krawczyk, Adalbert
    Zettler, Markus
    Dolff, Sebastian
    Westhoff, Timm H.
    Rohn, Hana
    Stervbo, Ulrik
    Witzke, Oliver
    Babel, Nina
    FRONTIERS IN IMMUNOLOGY, 2022, 13
  • [25] Household transmission of COVID-19 cases associated with SARS-CoV-2 delta variant (B.1.617.2): national case-control study
    Allen, Hester
    Vusirikala, Amoolya
    Flannagan, Joe
    Twohig, Katherine A.
    Zaidi, Asad
    Chudasama, Dimple
    Lamagni, Theresa
    Groves, Natalie
    Turner, Charlie
    Rawlinson, Christopher
    Lopez-Bernal, Jamie
    Harris, Ross
    Charlett, Andre
    Dabrera, Gavin
    Kall, Meaghan
    LANCET REGIONAL HEALTH-EUROPE, 2022, 12
  • [26] Humoral Response Kinetics and Cross-Immunity in Hospitalized Patients with SARS-CoV-2 WT, Delta, or Omicron Infections: A Comparison between Vaccinated and Unvaccinated Cohorts
    Kang, Hyunhye
    Lee, Jihyun
    Jung, Jin
    Oh, Eun-Jee
    VACCINES, 2023, 11 (12)
  • [27] Changing Features of COVID-19: Characteristics of Infections with the SARS-CoV-2 Delta (B.1.617.2) and Alpha (B.1.1.7) Variants in Southern Italy
    Loconsole, Daniela
    Centrone, Francesca
    Morcavallo, Caterina
    Campanella, Silvia
    Accogli, Marisa
    Sallustio, Anna
    Peccarisi, Davide
    Stufano, Angela
    Lovreglio, Piero
    Chironna, Maria
    VACCINES, 2021, 9 (11)
  • [28] SARS-CoV-2 Delta (B.1.617.2) Variant: A Unique T478K Mutation in Receptor Binding Motif (RBM) of Spike Gene
    Jhun, Hyunjhung
    Park, Ho-Young
    Hisham, Yasmin
    Song, Chang-Seon
    Kim, Soohyun
    IMMUNE NETWORK, 2021, 21 (05)
  • [29] SARS-CoV-2 mRNA Vaccine Breakthrough Infections in Fully Vaccinated Healthcare Personnel: A Systematic Review
    Ledda, Caterina
    Costantino, Claudio
    Motta, Giuseppe
    Cunsolo, Rosario
    Stracquadanio, Patrizia
    Liberti, Giuseppe
    Maltezou, Helena C.
    Rapisarda, Venerando
    TROPICAL MEDICINE AND INFECTIOUS DISEASE, 2022, 7 (01)
  • [30] Comparison of the clinical characteristics of SARS-CoV-2 Delta (B.1.617.2) and Omicron (B.1.1.529) infected patients from a single hospitalist service
    Radhakrishnan, N.
    Liu, M.
    Idowu, B.
    Bansari, A.
    Rathi, K.
    Magar, S.
    Mundhra, L.
    Sarmiento, J.
    Ghaffar, U.
    Kattan, J.
    Jones, R.
    George, J.
    Yang, Y.
    Southwick, F.
    BMC INFECTIOUS DISEASES, 2023, 23 (01)