C. Chae, Porcine respiratory disease complex: Interaction of vaccination and porcine circovirus type 2, porcine reproductive and respiratory syndrome virus, and Mycoplasma hyopneumoniae, Vet J, vol.212, pp.1-6, 2016.

J. E. Butler, Porcine reproductive and respiratory syndrome (PRRS): an immune dysregulatory pandemic, Immunol Res, vol.59, pp.81-108, 2014.

F. Meurens, A. Summerfield, H. Nauwynck, L. Saif, and V. Gerdts, The pig: a model for human infectious diseases, Trends Microbiol, vol.20, pp.50-57, 2012.

P. Maisonnasse, The respiratory DC/macrophage network at steady-state and upon influenza infection in the swine biomedical model, Mucosal Immunol, vol.9, pp.835-849, 2016.
URL : https://hal.archives-ouvertes.fr/hal-02394068

P. Maisonnasse, E. Bordet, E. Bouguyon, and N. Bertho, Broncho Alveolar Dendritic Cells and Macrophages Are Highly Similar to Their Interstitial Counterparts, PLoS One, vol.11, 2016.
URL : https://hal.archives-ouvertes.fr/hal-01602503

B. V. Patel, K. C. Tatham, M. R. Wilson, K. P. O'dea, and M. Takata, In vivo compartmental analysis of leukocytes in mouse lungs, Am J Physiol Lung Cell Mol Physiol, vol.309, pp.639-652, 2015.

Y. Cai, In vivo characterization of alveolar and interstitial lung macrophages in rhesus macaques: implications for understanding lung disease in humans, J Immunol, vol.192, pp.2821-2829, 2014.

K. E. Longworth, The comparative biology of pulmonary intravascular macrophages, Front Biosci, vol.2, pp.232-241, 1997.

J. D. Brain, R. M. Molina, M. M. Decamp, and A. E. Warner, Pulmonary intravascular macrophages: their contribution to the mononuclear phagocyte system in 13 species, Am J Physiol, vol.276, pp.146-154, 1999.

O. S. Atwal and K. A. Saldanha, Erythrophagocytosis in alveolar capillaries of goat lung: ultrastructural properties of blood monocytes, Acta Anat (Basel), vol.124, pp.245-254, 1985.

A. E. Warner, B. E. Barry, and J. D. Brain, Pulmonary intravascular macrophages in sheep. Morphology and function of a novel constituent of the mononuclear phagocyte system, Lab Invest, vol.55, pp.276-288, 1986.

, Scientific REPORts |, vol.8, 2018.

A. E. Warner and J. D. Brain, Intravascular pulmonary macrophages: a novel cell removes particles from blood, Am J Physiol, vol.250, pp.728-732, 1986.

L. Carrasco, Pulmonary intravascular macrophages in deer, Vet Res, vol.27, pp.71-77, 1996.
URL : https://hal.archives-ouvertes.fr/hal-00902400

M. Kawashima, M. Kuwamura, M. Takeya, and J. Yamate, Morphologic characteristics of pulmonary macrophages in cetaceans: particular reference to pulmonary intravascular macrophages as a newly identified type, Vet Pathol, vol.41, pp.682-686, 2004.

N. C. Staub, Pulmonary intravascular macrophages, Annu Rev Physiol, vol.56, pp.47-67, 1994.

L. Carrasco, African swine fever: Expression of interleukin-1 alpha and tumour necrosis factor-alpha by pulmonary intravascular macrophages, J Comp Pathol, vol.126, pp.194-201, 2002.

O. P. Parbhakar, T. Duke, H. G. Townsend, and B. Singh, Depletion of pulmonary intravascular macrophages partially inhibits lipopolysaccharide-induced lung inflammation in horses, Vet Res, vol.36, pp.557-569, 2005.
URL : https://hal.archives-ouvertes.fr/hal-00902983

B. Singh, J. W. Pearce, L. N. Gamage, K. Janardhan, and S. Caldwell, Depletion of pulmonary intravascular macrophages inhibits acute lung inflammation, Am J Physiol Lung Cell Mol Physiol, vol.286, pp.363-372, 2004.

Z. T. Chen, LPS induces pulmonary intravascular macrophages producing inflammatory mediators via activating NF-kappaB, J Cell Biochem, vol.89, pp.1206-1214, 2003.

C. G. Chitko-mckown, Porcine alveolar and pulmonary intravascular macrophages: comparison of immune functions, J Leukoc Biol, vol.50, pp.364-372, 1991.

S. Gory, The vascular endothelial-cadherin promoter directs endothelial-specific expression in transgenic mice, Blood, vol.93, pp.184-192, 1999.

C. Schulz, A lineage of myeloid cells independent of Myb and hematopoietic stem cells, Science, vol.336, pp.86-90, 2012.

M. Guilliams, Alveolar macrophages develop from fetal monocytes that differentiate into long-lived cells in the first week of life via GM-CSF, J Exp Med, vol.210, 1977.

G. Auray, Characterization and Transcriptomic Analysis of Porcine Blood Conventional and Plasmacytoid Dendritic Cells Reveals Striking Species-Specific Differences, J Immunol, vol.197, pp.4791-4806, 2016.

S. Moreno, Porcine monocyte subsets differ in the expression of CCR2 and in their responsiveness to CCL2, Vet Res, vol.41, 2010.
URL : https://hal.archives-ouvertes.fr/hal-00903204

A. Aziz, E. Soucie, S. Sarrazin, and M. H. Sieweke, MafB/c-Maf deficiency enables self-renewal of differentiated functional macrophages, Science, vol.326, pp.867-871, 2009.
URL : https://hal.archives-ouvertes.fr/hal-00430871

U. U. Karniychuk, Pathogenesis and antigenic characterization of a new East European subtype 3 porcine reproductive and respiratory syndrome virus isolate, BMC Vet Res, vol.6, 2010.

P. Renson, Dynamic changes in bronchoalveolar macrophages and cytokines during infection of pigs with a highly or low pathogenic genotype 1 PRRSV strain, Vet Res, vol.48, 2017.
URL : https://hal.archives-ouvertes.fr/hal-01499747

P. Renson, Preparation for emergence of an Eastern European porcine reproductive and respiratory syndrome virus (PRRSV) strain in Western Europe: Immunization with modified live virus vaccines or a field strain confers partial protection, Vet Microbiol, vol.204, pp.133-140, 2017.

D. Morton and T. A. Bertram, Isolation and preliminary in vitro characterization of the porcine pulmonary intravascular macrophage, J Leukoc Biol, vol.43, pp.403-410, 1988.

R. Thanawongnuwech, E. L. Thacker, and P. G. Halbur, Effect of porcine reproductive and respiratory syndrome virus (PRRSV) (isolate ATCC VR-2385) infection on bactericidal activity of porcine pulmonary intravascular macrophages (PIMs): in vitro comparisons with pulmonary alveolar macrophages (PAMs), Vet Immunol Immunopathol, vol.59, pp.323-335, 1997.

R. Thanawongnuwech, P. G. Halbur, M. R. Ackermann, E. L. Thacker, and R. L. Royer, Effects of low (modified-live virus vaccine) and high (VR-2385)-virulence strains of porcine reproductive and respiratory syndrome virus on pulmonary clearance of copper particles in pigs, Vet Pathol, vol.35, pp.398-406, 1998.

S. Ensan, Self-renewing resident arterial macrophages arise from embryonic CX3CR1(+) precursors and circulating monocytes immediately after birth, Nat Immunol, vol.17, pp.159-168, 2016.

E. Cantu, Depletion of pulmonary intravascular macrophages prevents hyperacute pulmonary xenograft dysfunction, Transplantation, vol.81, pp.1157-1164, 2006.

W. J. Shih, P. A. Domstad, B. Friedman, and F. H. Deland, Intrathoracic abnormalities demonstrated by technetium-99m sulfur colloid imaging, Clin Nucl Med, vol.11, pp.792-796, 1986.

D. J. Dehring and B. L. Wismar, Intravascular macrophages in pulmonary capillaries of humans, Am Rev Respir Dis, vol.139, pp.1027-1029, 1989.

W. C. Klingensmith, S. L. Yang, and H. N. Wagner, Lung uptake of Tc-99m sulfur colloid in liver and spleen imaging, J Nucl Med, vol.19, pp.31-35, 1978.

S. S. Gill, Role of pulmonary intravascular macrophages in endotoxin-induced lung inflammation and mortality in a rat model, Respir Res, vol.9, 2008.

K. E. Longworth, A. M. Westgate, M. K. Grady, J. Y. Westcott, and N. C. Staub, Development of pulmonary intravascular macrophage function in newborn lambs, J Appl Physiol, vol.73, pp.2608-2615, 1985.

E. L. Soucie, Lineage-specific enhancers activate self-renewal genes in macrophages and embryonic stem cells, Science, vol.351, 2016.
URL : https://hal.archives-ouvertes.fr/hal-01438535

V. Horak, K. Fortyn, V. Hruban, and J. Klaudy, Hereditary melanoblastoma in miniature pigs and its successful therapy by devitalization technique, Cell Mol Biol, vol.45, pp.1119-1129, 1999.