# Editorial: Community series in the role of complement in health and disease, volume II

**Authors:** Maciej Cedzyński, Thomas Vorup-Jensen, Marcin Okrój, Anna S. Świerzko

PMC · DOI: 10.3389/fimmu.2025.1658763 · Frontiers in Immunology · 2025-07-17

## Full-text entities

- **Genes:** C1QBP (complement C1q binding protein) [NCBI Gene 708] {aka COXPD33, GC1QBP, HABP1, SF2AP32, SF2p32, gC1Q-R}, BDKRB1 (bradykinin receptor B1) [NCBI Gene 623] {aka B1BKR, B1R, BKB1R, BKR1, BRADYB1}, Masp1 (MBL associated serine protease 1) [NCBI Gene 17174] {aka CCPII, Crarf, Masp1/3}, COLEC12 (collectin subfamily member 12) [NCBI Gene 81035] {aka CLP1, NSR2, SCARA4, SRCL}, C3AR1 (complement C3a receptor 1) [NCBI Gene 719] {aka AZ3B, C3AR, HNFAG09}, Cfh (complement component factor h) [NCBI Gene 12628] {aka Mud-1, NOM, Sas-1, Sas1}, COLEC11 (collectin subfamily member 11) [NCBI Gene 78989] {aka 3MC2, CL-11, CL-K1-I, CL-K1-II, CL-K1-IIa, CL-K1-IIb}, CFH (complement factor H) [NCBI Gene 3075] {aka AHUS1, AMBP1, ARMD4, ARMS1, CFHL3, FH}, NLRP3 (NLR family pyrin domain containing 3) [NCBI Gene 114548] {aka AGTAVPRL, AII, AVP, C1orf7, CIAS1, CLR1.1}, KLK4 (kallikrein related peptidase 4) [NCBI Gene 9622] {aka AI2A1, ARM1, EMSP, EMSP1, KLK-L1, PRSS17}, MBL2 (mannose binding lectin 2) [NCBI Gene 4153] {aka COLEC1, HSMBPC, MBL, MBL2D, MBP, MBP-C}, C1QC (complement C1q C chain) [NCBI Gene 714] {aka C1Q-C, C1QD3, C1QG}, C1QA (complement C1q A chain) [NCBI Gene 712] {aka C1QD1}, CFHR3 (complement factor H related 3) [NCBI Gene 10878] {aka CFHL3, DOWN16, FHR-3, FHR3, HLF4}, CD68 (CD68 molecule) [NCBI Gene 968] {aka GP110, LAMP4, SCARD1}, CD59 (CD59 molecule (CD59 blood group)) [NCBI Gene 966] {aka 16.3A5, 1F5, EJ16, EJ30, EL32, G344}, COLEC10 (collectin subfamily member 10) [NCBI Gene 10584] {aka 3MC3, CL-10, CL-34, CLL1}, Agtrap (angiotensin II, type I receptor-associated protein) [NCBI Gene 11610] {aka 3300002E14Rik, AT1R, Atrap, D4Wsu124e}, Cfhr3 (complement factor H-related 3) [NCBI Gene 624286] {aka EG624286}, N (nucleocapsid phosphoprotein) [NCBI Gene 43740575], MASP2 (MBL associated serine protease 2) [NCBI Gene 10747] {aka MAP-2, MAP19, MASP-2, MASP1P1, sMAP}, C5AR1 (complement C5a receptor 1) [NCBI Gene 728] {aka C5A, C5AR, C5R1, CD88}, EEF1A1 (eukaryotic translation elongation factor 1 alpha 1) [NCBI Gene 1915] {aka CCS-3, CCS3, EE1A1, EEF-1, EEF1A, EF-Tu}, C1QB (complement C1q B chain) [NCBI Gene 713] {aka C1QD2}, C3 (complement C3) [NCBI Gene 718] {aka AHUS5, ARMD9, ASP, C3a, C3b, CPAMD1}, Cfhr1 (complement factor H-related 1) [NCBI Gene 50702] {aka CFHRB, Cfhl1, Fhr1, muFHR1}
- **Diseases:** dyslipidemia (MESH:D050171), FD (MESH:D000795), RPE depigmentation (MESH:C536309), hypertension (MESH:D006973), aeruginosa (MESH:D011552), Complement (MESH:D007153), leukaemias (MESH:D015458), pelvic pain (MESH:D017699), autoimmune disease (MESH:D001327), dyspareunia (MESH:D004414), multiple myeloma (MESH:D009101), AMD (MESH:D006009), reperfusion injury (MESH:D015427), obesity (MESH:D009765), aggression (MESH:D010554), endometrial lesions (MESH:D014591), ischemia (MESH:D007511), multiple organ failure (MESH:D009102), heart failure (MESH:D006333), dysmenorrhea (MESH:D004412), atrophy (MESH:D001284), IgA nephropathy (MESH:D005922), renal diseases (MESH:D007674), atherosclerosis (MESH:D050197), endometrial ovarian cysts (MESH:C536396), preterm births (MESH:D047928), carcinogenesis (MESH:D063646), prematurity (MESH:C536271), PE (MESH:D011225), shock (MESH:D012769), MN (MESH:D015433), aortic aneurysm (MESH:D001014), cardiovascular and metabolic diseases (MESH:D002318), steatotic liver disease (MESH:D008107), diabetic cardiomyopathy (MESH:D058065), C (OMIM:211750), proteinuria (MESH:D011507), EM (MESH:D004715), pulmonary inflammation (MESH:D011014), smoking- (MESH:D015208), infertility (MESH:D007246), deaths (MESH:D003643), hypersensitivity (MESH:D004342), cancer (MESH:D009369), age-related macular degeneration (MESH:D008268), chronic inflammation (MESH:D007249), infection (MESH:D007239), thromboinflammation (MESH:D000090882), metabolic dysfunction (MESH:D008659), gynaecological disorder (MESH:D009358), growth restriction (MESH:D005317), interstitial fibrosis (MESH:D005355), acute myeloid leukaemia (MESH:D054218), RDS (MESH:D012128), coagulopathy (MESH:D001778), coronary heart disease (MESH:D003327), Systemic sclerosis (MESH:D012595), arrhythmia (MESH:D001145), lymphomas (MESH:D008223), dyschezia (MESH:D003248)
- **Chemicals:** hydroquinone (MESH:C031927), NaIO3 (MESH:C032285), heavy (-), C (MESH:D002244), carbohydrate (MESH:D002241), lipid (MESH:D008055)
- **Species:** Apis mellifera scutellata (African honeybee, subspecies) [taxon 212527], Pseudomonas aeruginosa (species) [taxon 287], Apis mellifera (bee, species) [taxon 7460], Homo sapiens (human, species) [taxon 9606], Nicotiana tabacum (American tobacco, species) [taxon 4097], Mus musculus (house mouse, species) [taxon 10090], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]
- **Mutations:** Y402H
- **Cell lines:** RPE — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_IQ82)

## Full text

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Source: https://tomesphere.com/paper/PMC12310669